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  • 928-96-1 Structure
  • Basic information

    1. Product Name: Leaf alcohol
    2. Synonyms: (3Z)-3-Hexen-1-ol;(z)-3-hexen-1-o;(Z)-3-Hexen-1-ol;(Z)-Hex-3-en-1-ol;(Z)-Hex-3-ene-1-ol;(Z)Hex-3-enol;1-Hydroxyhex-3-ene;3-(Z)-Hexenol
    3. CAS NO:928-96-1
    4. Molecular Formula: C6H12O
    5. Molecular Weight: 100.16
    6. EINECS: 213-192-8
    7. Product Categories: Pharmaceutical Intermediates;alcohol Flavor;G-H;Alphabetical Listings;Flavors and Fragrances;Acyclic;Alkenes;Organic Building Blocks;Certified Natural ProductsFlavors and Fragrances;Building Blocks;Carthamus tinctorius (Safflower oil);Chemical Synthesis;Citrus aurantium (Seville orange);Nutrition Research;Ocimum basilicum (Basil);Organic Building Blocks;Phytochemicals by Plant (Food/Spice/Herb);Zingiber officinale (Ginger);Cosmetics
    8. Mol File: 928-96-1.mol
    9. Article Data: 62
  • Chemical Properties

    1. Melting Point: 22.55°C (estimate)
    2. Boiling Point: 156-157 °C(lit.)
    3. Flash Point: 112 °F
    4. Appearance: APHA: ≤100/Liquid
    5. Density: 0.848 g/mL at 25 °C(lit.)
    6. Vapor Density: 3.45 (vs air)
    7. Vapor Pressure: 1.04mmHg at 25°C
    8. Refractive Index: n20/D 1.44(lit.)
    9. Storage Temp.: Flammables area
    10. Solubility: N/A
    11. PKA: 15.00±0.10(Predicted)
    12. Water Solubility: INSOLUBLE
    13. Stability: Stable. Substances to be avoided include strong oxidizing agents and strong acids. Flammable.
    14. Merck: 14,4700
    15. BRN: 1719712
    16. CAS DataBase Reference: Leaf alcohol(CAS DataBase Reference)
    17. NIST Chemistry Reference: Leaf alcohol(928-96-1)
    18. EPA Substance Registry System: Leaf alcohol(928-96-1)
  • Safety Data

    1. Hazard Codes: F
    2. Statements: 10
    3. Safety Statements: 16
    4. RIDADR: UN 1987 3/PG 3
    5. WGK Germany: 1
    6. RTECS: MP8400000
    7. F: 10
    8. TSCA: Yes
    9. HazardClass: 3
    10. PackingGroup: III
    11. Hazardous Substances Data: 928-96-1(Hazardous Substances Data)

928-96-1 Usage

Description

Leaf alcohol, also known as cis-3-hexen-1-ol, is a primary alcohol that consists of (3Z)-hex-3-ene substituted by a hydroxy group at position 1. It is a colorless liquid with a characteristic odor of freshly cut grass and green leaves. Leaf alcohol is found in green tea, violet leaf oil, and many types of leaves, herbs, and grasses. It is one of the key volatile constituents of green leaf volatiles (GLV) that can act as an attractant to various insects and is emitted by green plants when they are physically damaged.

Uses

Used in Perfumery:
Leaf alcohol is used as a floral fragrance in perfumery for its characteristic odor of green leaves.
Used in Flavor Industry:
Leaf alcohol is used to obtain natural green top notes in perfumes and flavors, contributing to the fresh, green, and raw fruity taste with a pungent depth.
Used in Synthesis:
Leaf alcohol serves as the starting material for the synthesis of (2E,6Z)-2,6-nonadien-1-ol and (2E,6Z)-2,6-nonadien-1-al, which are important compounds in the flavor and fragrance industry.
Used in Biotechnology:
Biotechnological processes have been developed for the synthesis of leaf alcohol as a natural flavor compound.
Leaf alcohol is also investigated for its antidiabetic activity, indicating potential use in pharmaceutical applications.

Preparation

By the reaction of butyne-1 with ethylene oxide and subsequent selective reduction to the eis isomer (Bedoukian, 1967).

Flammability and Explosibility

Flammable

Synthesis

Extracted from various essential oils and purified by reacting it to the corresponding phthalate or allophanate; it was synthesized by Ruzi-ka and Schinz, who also clarified its chemical structure; Stoll and Rouve reported on the most significant differences between the natural and the synthetic products (Burdock, 1995)

References

[1] NPCS Board of Consultants & Engineers, Industrial Alcohol of Technology Handbook, 2010 [2] A. Shirwaikar, K. Rajendran and C. Kumar, Oral Antidiabetic Activity of Annona squamosa Leaf Alcohol Extract in NIDDM Rats, Pharmaceutical Biology, 2004, vol. 42, 30-35

Check Digit Verification of cas no

The CAS Registry Mumber 928-96-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 928-96:
(5*9)+(4*2)+(3*8)+(2*9)+(1*6)=101
101 % 10 = 1
So 928-96-1 is a valid CAS Registry Number.

928-96-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-hex-3-en-1-ol

1.2 Other means of identification

Product number -
Other names cis-3-Hexen-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Fragrances
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:928-96-1 SDS

928-96-1Synthetic route

3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
With hydrogen; N,N′-bis(salicylidene)-ethylenediamino‑palladium In pyridine for 0.283333h;100%
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760.051 Torr;99%
With trichlorosilane; silica gel; acetic acid; tetrakis(triphenylphosphine) palladium(0) In dichloromethane for 3h; Ambient temperature;96%
3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

hexan-1-ol
111-27-3

hexan-1-ol

Conditions
ConditionsYield
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics;A 99%
B n/a
With hydrogen In methanol at 30℃; under 760.051 Torr; for 3h;A 99%
B 1%
With hydrogen In methanol at 20℃; under 150.015 - 900.09 Torr; for 0.0116667h; Inert atmosphere; Schlenk technique; Green chemistry;A n/a
B n/a
2,4-hexadiene-1-ol
111-28-4

2,4-hexadiene-1-ol

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

D

hexan-1-ol
111-27-3

hexan-1-ol

Conditions
ConditionsYield
With hydrogen; (methyl benzoate)Cr(CO)6 In methanol at 190 - 200℃; under 36775.4 Torr; for 2h;A 92.5%
B 4.6%
C 2.3%
D 0.6%
With hydrogen; (1,2,4,5-tetramethylbenzene)tricarbonylchromium(0) In methanol at 190 - 200℃; under 36775.4 Torr; for 4h; Product distribution; other arene ligands, other solvents; also in absence of arene ligands;
3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

C

hexan-1-ol
111-27-3

hexan-1-ol

Conditions
ConditionsYield
With hydrogen In methanol at 20℃; under 1800.18 Torr; Catalytic behavior; Reagent/catalyst;A 88%
B n/a
C n/a
With hydrogen; poly(N-vinyl-2-pyrrolidone)-stabilised Pd-nanoclusters In methanol at 29℃;
With hydrogen In isopropyl alcohol at 30℃; under 2250.23 Torr; for 20h; Autoclave; optical yield given as %de; stereoselective reaction;
Sorbyl alcohol
17102-64-6

Sorbyl alcohol

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
With Na12(Ga4(1,5-bis(2,3-dihydroxybenzamido)naphthalene))6; [(DMPE)Rh(COD)][BF4]; hydrogen In water-d2 at 20℃; for 12h;84%
With hydrogen; chromium(0) hexacarbonyl In hexane at 160 - 180℃; under 38000 - 60800 Torr; for 4h;
With hydrogen; [(η5-C5Me5)Ru(η4-MeCH=CHCH=CHCO2H)] triflate In ethylene glycol at 40℃; under 15001.5 Torr; for 0.42h; Catalytic hydrogenation;
(3Z)-hexenal
6789-80-6

(3Z)-hexenal

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
With 1% Rh/Al2O3; hydrogen; iron In ethanol at 120℃; under 15001.5 Torr; for 4h; Reagent/catalyst; Temperature; Pressure; Solvent; Autoclave;80.35%
With aldehyde reductase; nicotinamide adenine dinucleotide phosphate Enzymatic reaction;
6-methyl-3,6-dihydro-2H-pyran
55230-25-6

6-methyl-3,6-dihydro-2H-pyran

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
With calcium; ethylenediamine at 90℃; for 8h;60%
homoalylic alcohol
627-27-0

homoalylic alcohol

diethylaluminium chloride
96-10-6

diethylaluminium chloride

A

3-methyl-1-pentanol
589-35-5, 20281-83-8

3-methyl-1-pentanol

B

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

C

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

D

butan-1-ol
71-36-3

butan-1-ol

E

hexan-1-ol
111-27-3

hexan-1-ol

Conditions
ConditionsYield
With titanium tetrachloride In dichloromethane at -45℃; for 2h; Mechanism; Product distribution; variation of added base;A 13%
B 3%
C 18%
D 20%
E 21%
3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
With Pd-BaSO4; benzene at 50℃; Hydrogenation;
With lithium; Trimethylenediamine at 25℃; for 2h;
With palladium/highly-ordered mesoporous silica supported 3-D pore network(3.7) 1-phenylethan-1-amine 0.02 for 2.91667h;
With hydrogen In methanol at 20℃; under 862.586 Torr; for 8h; Catalytic behavior; Flow reactor;A n/a
B n/a
cis/trans-3-chloro-2-ethyltetrahydrofuran
98486-14-7

cis/trans-3-chloro-2-ethyltetrahydrofuran

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
With samarium diiodide In tetrahydrofuran Product distribution; Heating; using dipolar-aprotic cosolvents;
With samarium diiodide In tetrahydrofuran for 5h; Heating; Yield given. Yields of byproduct given;
6-methyl-3,6-dihydro-2H-pyran
55230-25-6

6-methyl-3,6-dihydro-2H-pyran

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

C

(E)-hex-4-en-1-ol
928-92-7

(E)-hex-4-en-1-ol

Conditions
ConditionsYield
With lithium In various solvent(s) at -78℃; Yield given. Yields of byproduct given;
5-methyl-2-thiophenemethanol
63826-59-5

5-methyl-2-thiophenemethanol

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
With lithium In various solvent(s) Yield given. Yields of byproduct given. Title compound not separated from byproducts;
formaldehyd
50-00-0

formaldehyd

1-penten
109-67-1

1-penten

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
dimethylaluminum chloride In n-heptane; dichloromethane at 25℃; Yield given. Yields of byproduct given;
3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

C

4-hexyn-1-ol
928-93-8

4-hexyn-1-ol

D

hexan-1-ol
111-27-3

hexan-1-ol

Conditions
ConditionsYield
With lithium; Trimethylenediamine at 60℃; for 1.33333h; Product distribution; other compounds containing a triple bond and/or an aromatic ring; var. temp., time;
(3R,4R)-3,4-Dibromo-hexan-1-ol
78076-11-6, 89583-13-1

(3R,4R)-3,4-Dibromo-hexan-1-ol

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
With tetrabutylammonium tetrafluoroborate In N,N-dimethyl-formamide -1.4 V (vs. SCE) at a mercury pool (divided cell); Yield given;
2-Chlorobutanal
28832-55-5

2-Chlorobutanal

ethyl acetate
141-78-6

ethyl acetate

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
3-chloro-2-vinyltetrahydrofuran
102067-72-1, 102067-73-2

3-chloro-2-vinyltetrahydrofuran

A

5-Hexen-1-ol
821-41-0

5-Hexen-1-ol

B

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

C

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

D

(E)-hex-4-en-1-ol
928-92-7

(E)-hex-4-en-1-ol

Conditions
ConditionsYield
With sodium In diethyl ether Yield given. Yields of byproduct given;
With sodium In toluene Yield given. Yields of byproduct given;
2-hydroxymethyl-5-methyl-2,5-dihydrothiophene
74379-24-1

2-hydroxymethyl-5-methyl-2,5-dihydrothiophene

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
With lithium In various solvent(s) Yield given. Yields of byproduct given. Title compound not separated from byproducts;
2,4-hexadiene-1-ol
111-28-4

2,4-hexadiene-1-ol

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
With hydrogen; chromium(0) hexacarbonyl In methanol at 190 - 200℃; under 36775.4 Torr; for 4h; Yield given. Yields of byproduct given;
With hydrogen; [Ru(C5(1,2,4-tBu3)H2)(1,3-COD)]BF4 In acetone at 70℃; under 3750.38 Torr; Product distribution / selectivity;
With diphenyl-phosphinic acid; hydrogen; [Ru(C5(1,2,4-tBu3)H2)(1,3-COD)]BF4 In acetone at 70℃; under 3750.38 Torr; Product distribution / selectivity;
methyl (Z)-hex-3-enoate
13894-62-7

methyl (Z)-hex-3-enoate

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
With sodium hydroxide; sodium tetrahydroborate; zinc 2-ethylhexanoate 1.) THF, 70 deg C, 4 h, 2.) 40 deg, 1 h; Yield given; Multistep reaction;
diethyl ether
60-29-7

diethyl ether

3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

hydrogen

hydrogen

palladium-barium sulfate

palladium-barium sulfate

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
at -18℃; Hydrogenation;
tetrachloromethane
56-23-5

tetrachloromethane

3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

palladium-barium sulfate

palladium-barium sulfate

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
at 100℃; Hydrogenation;
3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

benzene
71-43-2

benzene

palladium-barium sulfate

palladium-barium sulfate

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
at 50℃; Hydrogenation;
3-hexyn-1-ol
1002-28-4

3-hexyn-1-ol

water
7732-18-5

water

palladium

palladium

A

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

B

(E)-3-hexen-1-ol
928-97-2

(E)-3-hexen-1-ol

Conditions
ConditionsYield
at 21 - 23℃; under 843 Torr; Hydrogenation;
trans,trans-2,4-Hexadienal
142-83-6

trans,trans-2,4-Hexadienal

2-vinyl-trans(?)-crotonaldehyde

2-vinyl-trans(?)-crotonaldehyde

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NaBH4 / H2O / 2 h / Ambient temperature
2: H2 / Cr(CO)6 / methanol / 4 h / 190 - 200 °C / 36775.4 Torr
View Scheme
Multi-step reaction with 2 steps
1: NaBH4 / H2O / 2 h / Ambient temperature
2: 92.5 percent / H2 / (methyl benzoate)Cr(CO)6 / methanol / 2 h / 190 - 200 °C / 36775.4 Torr
View Scheme
2-methylthiophene-5-carboxylic acid
1918-79-2

2-methylthiophene-5-carboxylic acid

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
2: LiAlH4 / diethyl ether
3: Li / various solvent(s)
View Scheme
methyl 5-methylthiophene-2-carboxylate
19432-69-0

methyl 5-methylthiophene-2-carboxylate

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: LiAlH4 / diethyl ether
2: Li / various solvent(s)
View Scheme
5-methyl-2,5-dihydrothiophene-2-carboxylic acid
71624-90-3

5-methyl-2,5-dihydrothiophene-2-carboxylic acid

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
2: LiAlH4 / diethyl ether
3: Li / various solvent(s)
View Scheme
Methyl 2,5-Dihydro-5-methyl-2-thiophenecarboxylate
71624-92-5

Methyl 2,5-Dihydro-5-methyl-2-thiophenecarboxylate

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: LiAlH4 / diethyl ether
2: Li / various solvent(s)
View Scheme
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide
18303-04-3

N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide

1,1-dimethylethyl (Z)-3-hexenyl[(4-methylphenyl)sulfonyl]carbamate
126745-58-2

1,1-dimethylethyl (Z)-3-hexenyl[(4-methylphenyl)sulfonyl]carbamate

Conditions
ConditionsYield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0℃;100%
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran for 3h; Ambient temperature;88%
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; for 6h; Mitsunobu reaction;74%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

2-Bromoacetyl bromide
598-21-0

2-Bromoacetyl bromide

(Z)-3-hexenyl bromoacetate
90448-99-0

(Z)-3-hexenyl bromoacetate

Conditions
ConditionsYield
With pyridine In dichloromethane100%
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0℃;
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

triphenylphosphine
603-35-0

triphenylphosphine

(Z)-hex-3-en-1-yliodotriphenyl-λ5-phosphane

(Z)-hex-3-en-1-yliodotriphenyl-λ5-phosphane

Conditions
ConditionsYield
Stage #1: (Z)-3-Hexen-1-ol; triphenylphosphine With 1H-imidazole In dichloromethane at 0℃; for 0.333333h;
Stage #2: With iodine In dichloromethane at 0 - 20℃; for 3h;
Stage #3: triphenylphosphine In acetonitrile for 19h; Reflux;
100%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

2-(3-ethyloxiran-2-yl)ethan-1-ol
67663-02-9

2-(3-ethyloxiran-2-yl)ethan-1-ol

Conditions
ConditionsYield
With tert.-butylhydroperoxide; C14H17BrMoN2O2 In dichloromethane at 54.84℃; for 24h; Reagent/catalyst;99%
With Oxone; ethylenediaminetetraacetic acid; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; acetone In water; acetonitrile for 4h;90%
With dihydrogen peroxide; sodium acetate; ortho-tungstic acid In methanol; water at 20℃; for 16h; pH=4.5;49%
succinic acid anhydride
108-30-5

succinic acid anhydride

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

4-[(Z)-3-hexenyloxy]-4-oxobutanoic acid

4-[(Z)-3-hexenyloxy]-4-oxobutanoic acid

Conditions
ConditionsYield
zinc(II) perchlorate In diethyl ether for 7h; Heating;99%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

acetic anhydride
108-24-7

acetic anhydride

(Z)-3-Hexenyl acetate
3681-71-8

(Z)-3-Hexenyl acetate

Conditions
ConditionsYield
zinc(II) perchlorate at 20℃; for 1.83333h;99%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

triisopropylsilyl chloride
13154-24-0

triisopropylsilyl chloride

(Z)-(hex-3-en-1-yloxy)triisopropylsilane

(Z)-(hex-3-en-1-yloxy)triisopropylsilane

Conditions
ConditionsYield
With 1H-imidazole In dichloromethane at 20℃; for 1h; Inert atmosphere;99%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

1-benzyloxyallene
67515-49-5

1-benzyloxyallene

(R,Z)-(((1-(hex-3-en-1-yloxy)allyl)oxy)methyl)benzene

(R,Z)-(((1-(hex-3-en-1-yloxy)allyl)oxy)methyl)benzene

Conditions
ConditionsYield
With trans-1,2-(1S,2S)-1,2-diaminocyclohexane-N,N’-bis(2’-diphenylphosphinobenzoyl); tris-(dibenzylideneacetone)dipalladium(0); triethylamine In dichloromethane at 20℃; for 20h; Inert atmosphere;99%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

methanesulfonic acid hex-3(Z)-enyl ester
79503-95-0

methanesulfonic acid hex-3(Z)-enyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 1.5h;98%
With triethylamine In dichloromethane for 0.5h; Ambient temperature;97%
With pyridine at 0 - 20℃; for 6h;91%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

[(Z)-3-hexenyl] tert-butyl carbonate

[(Z)-3-hexenyl] tert-butyl carbonate

Conditions
ConditionsYield
With zinc diacetate at 50℃; for 9h;98%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

acetic acid
64-19-7

acetic acid

(Z)-3-Hexenyl acetate
3681-71-8

(Z)-3-Hexenyl acetate

Conditions
ConditionsYield
With cobalt(II) chloride at 60℃; for 10h;97%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

diethyl (1-((4-methylphenyl)sulfonamido)prop-1-en-1-yl)phosphonate

diethyl (1-((4-methylphenyl)sulfonamido)prop-1-en-1-yl)phosphonate

diethyl ((Z)-1-((N-((Z)-hex-3-en-1-yl)-4-methylphenyl)sulfonamido)prop-1-en-1-yl)phosphonate

diethyl ((Z)-1-((N-((Z)-hex-3-en-1-yl)-4-methylphenyl)sulfonamido)prop-1-en-1-yl)phosphonate

Conditions
ConditionsYield
With tributylphosphine; di-isopropyl azodicarboxylate In tetrahydrofuran; toluene at 20℃; for 1h; Mitsunobu Displacement; Inert atmosphere;97%
styrene oxide
96-09-3

styrene oxide

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

(2R,3S,4R)-2-Benzyl-4-chloro-3-ethyl-tetrahydro-pyran

(2R,3S,4R)-2-Benzyl-4-chloro-3-ethyl-tetrahydro-pyran

Conditions
ConditionsYield
With indium(III) chloride In chloroform at 20℃; for 5h;96%
3,4-dihydro-2H-pyran
110-87-2

3,4-dihydro-2H-pyran

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

(Z)-2-(hex-3-en-1-yloxy)tetrahydro-2H-pyran

(Z)-2-(hex-3-en-1-yloxy)tetrahydro-2H-pyran

Conditions
ConditionsYield
With cerium(III) chloride; sodium iodide at 25℃; for 6h;96%
undec-10-enoyl chloride
38460-95-6

undec-10-enoyl chloride

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

(Z)-hex-3-en-1-yl undec-10-enoate

(Z)-hex-3-en-1-yl undec-10-enoate

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 20℃; for 4h;95%
With pyridine In dichloromethane at 0 - 20℃; for 4h;95%
With pyridine In dichloromethane at 0 - 20℃;95%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

mono-L-menthyl glutarate
220621-22-7

mono-L-menthyl glutarate

cis-3-hexenyl L-menthyl glutarate

cis-3-hexenyl L-menthyl glutarate

Conditions
ConditionsYield
With dmap; diisopropyl-carbodiimide In dichloromethane at 0 - 20℃;94%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

(3R,4R)-3,4-Dibromo-hexan-1-ol
78076-11-6, 89583-13-1

(3R,4R)-3,4-Dibromo-hexan-1-ol

Conditions
ConditionsYield
With pyridinium perbromide hydrobromide In chloroform at -60 - -10℃;93%
Conditions
ConditionsYield
With sodium hydroxide; dihydrogen peroxide; N-tosylimidazole In methanol for 3h;93%
With dihydrogen peroxide; ethenetetracarbonitrile In acetonitrile for 12h; Product distribution; Ambient temperature; other olefins, var. reagents (tetracyanoethylene oxide, carbonyl cyanide), var. temp.;92%
With dihydrogen peroxide; ethenetetracarbonitrile In acetonitrile for 12h; Ambient temperature;92%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

Benzoylformic acid
611-73-4

Benzoylformic acid

(Z)-3-hexenyl 2-oxo-2-phenylacetate
143618-83-1

(Z)-3-hexenyl 2-oxo-2-phenylacetate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 48h;93%
for 2h; Heating; Yield given;
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

(Z)-hex-3-en-1-yl sulfamate
450414-10-5

(Z)-hex-3-en-1-yl sulfamate

Conditions
ConditionsYield
With formic acid; isocyanate de chlorosulfonyle In N,N-dimethyl acetamide at 20℃;93%
With formic acid; isocyanate de chlorosulfonyle In N,N-dimethyl acetamide at 0 - 20℃;93%
With sulphamoyl chloride; triethylamine In acetonitrile at 0 - 23℃; Inert atmosphere;69%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

(3Z)-1-chloro-3-hexene
21676-01-7

(3Z)-1-chloro-3-hexene

Conditions
ConditionsYield
With thionyl chloride; N,N-dimethyl-formamide In dimethyl sulfoxide at 5 - 25℃; for 3h; Concentration;92%
With pyridine; thionyl chloride; chloroform
With pyridine; thionyl chloride In chloroform
With pyridine; thionyl chloride In hexane
Multi-step reaction with 2 steps
1: pyridine / CH2Cl2 / 16 h / 20 °C
2: 1.5 g / LiCl / acetone
View Scheme
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

trityl chloride
76-83-5

trityl chloride

cis-1-trityloxy-3-hexene
102952-59-0

cis-1-trityloxy-3-hexene

Conditions
ConditionsYield
With pyridine; dmap In dichloromethane for 24h;92%
With pyridine; benzene
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

tert-butylchlorodiphenylsilane
58479-61-1

tert-butylchlorodiphenylsilane

(Z)-tert-butyl(hex-3-en-1-yloxy)diphenylsilane
121353-04-6

(Z)-tert-butyl(hex-3-en-1-yloxy)diphenylsilane

Conditions
ConditionsYield
With 1H-imidazole; triethylamine In dichloromethane at 20℃; for 16h; Inert atmosphere;92%
With 1H-imidazole; diisopropylamine In dichloromethane for 40h; Ambient temperature;
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

3,4,5-trimethoxy-benzaldehyde
86-81-7

3,4,5-trimethoxy-benzaldehyde

C16H23IO4

C16H23IO4

Conditions
ConditionsYield
With iodine In dichloromethane at 23℃; for 0.583333h; Prins-cyclization;92%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

3,5-Bis(1,1-dimethylethyl)-4-methoxy-benzoic acid
93156-92-4

3,5-Bis(1,1-dimethylethyl)-4-methoxy-benzoic acid

(Z)-hex-3-en-1-yl 3,5-di-tert-butyl-4-methoxybenzoate

(Z)-hex-3-en-1-yl 3,5-di-tert-butyl-4-methoxybenzoate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; Inert atmosphere;92%
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

(Z)-3-hexenyl iodide
21676-03-9

(Z)-3-hexenyl iodide

Conditions
ConditionsYield
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 1h;91%
(i) TsCl, Py, (ii) NaI, acetone; Multistep reaction;
Multi-step reaction with 2 steps
1: 60 percent / pyridine / 8 h / 20 °C
2: NaI / acetonitrile / 3 h / 70 °C
View Scheme
(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

methyl 2-oxocyclopentane-1-carboxylate
10472-24-9

methyl 2-oxocyclopentane-1-carboxylate

2-Oxo-cyclopentanecarboxylic acid (Z)-hex-3-enyl ester

2-Oxo-cyclopentanecarboxylic acid (Z)-hex-3-enyl ester

Conditions
ConditionsYield
With N,N-3-diethylaminopropylated silica gel In xylene for 3.5h; Heating;91%

928-96-1Relevant articles and documents

Dahill

, p. 399 (1972)

Accelerated Semihydrogenation of Alkynes over a Copper/Palladium/Titanium (IV) Oxide Photocatalyst Free from Poison and H2 Gas

Imai, Shota,Nakanishi, Kousuke,Tanaka, Atsuhiro,Kominami, Hiroshi

, p. 1609 - 1616 (2020/02/15)

Selective hydrogenation of alkynes to alkenes (semihydrogenation) without the use of a poison and H2 is challenging because alkenes are easily hydrogenated to alkanes. In this study, a titanium (IV) oxide photocatalyst having Pd core-Cu shell nanoparticles (Pd@Cu/TiO2) was prepared by using the two-step photodeposition method, and Pd@Cu/TiO2 samples having various Cu contents were characterized by electron transmission microscopy, X-ray photoelectron spectroscopy and UV-vis spectroscopy. Thus-prepared Pd@Cu/TiO2 samples were used for photocatalytic hydrogenation of 4-octyne in alcohol and the catalytic properties were compared with those of Pd/TiO2 and Cu/TiO2. 4-Octyne was fully hydrogenated to octane over Pd/TiO2 at a high rate and 4-octyne was semihydrogenated to cis-4-octene over Cu/TiO2 at a low rate. Rapid semihydrogenation of 4-octyne was achieved over Pd(0.2 mol%)@Cu(1.0 mol%)/TiO2, indicating that the Pd core greatly activated the Cu shell that acted as reaction sites. A slight increase in the reaction temperature greatly increased the rate with a suppressed rate of H2 evolution as the side reaction. Changes in the reaction rates of the main and side reactions are discussed on the basis of results of kinetic studies. Reusability and expandability of Pd@Cu/TiO2 in semihydrogenation are also discussed.

Visible light-induced diastereoselective semihydrogenation of alkynes to cis-alkenes over an organically modified titanium(IV) oxide photocatalyst having a metal co-catalyst

Fukui, Makoto,Omori, Yuya,Kitagawa, Shin-ya,Tanaka, Atsuhiro,Hashimoto, Keiji,Kominami, Hiroshi

, p. 36 - 42 (2019/05/04)

Hydrogen (H2)-free and poison (lead and quinoline)-free semihydrogenation of alkynes to cis-alkenes under gentle conditions is one of the challenges to be solved. In this study, a titanium(IV) oxide photocatalyst having two functions (visible light responsiveness and semihydrogenation activity) was prepared by modification with 2,3-dihydroxynaphthalene (DHN) and a copper (Cu) co-catalyst, respectively. The photocatalyst (DHN/TiO2-Cu) showed high performance for diastereoselective semihydrogenation of alkynes to cis-alkenes in water-acetonitrile solution under visible light irradiation without the use of H2 and poisons. Alkynes having reducible functional groups were converted to the corresponding alkenes with the functional groups being preserved. The addition of water to acetonitrile changed the amount of alkynes adsorbed on the photocatalyst, which was a decisive factor determining the rate of hydrogenation. A relatively large apparent activation energy, 27 kJ mol?1, was obtained by a kinetic study, indicating that the rate-determining step of this reaction was not an electron production process but a thermal catalytic semihydrogenation process over the Cu co-catalyst. Semihydrogenation and hydrogen evolution occurred competitively on Cu metals and the former became predominant at slightly elevated temperatures, which is discussed on the basis of the kinetic parameters of two reactions.

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