334-88-3 Usage
Preparation
Diazomethane was generated with a diazomethane-generating glassware kit (Aldrich). A solution of N-methyl-N-nitroso-4-toluenesulfonamide (Diazald, 2.23 g, 10.4 mmol) in ether (24 mL) was added dropwise to a mixture of KOH (1.75 g, 31.2 mmol) in H2O (18 mL), ether (4 mL), and 2-(2-ethoxyethoxy)ethanol (18 mL) kept at 70 oC. The ethereal solution of diazomethane was continuously distilled into a flask that was ready to use for the next reaction.
Description
At room temperature, diazomethane (CH2N2) is a toxic yellow gas which can cause significant irritation upon inhalation. Solutions that contain concentrated diazomethane are highly toxic, and they can result in explosions. When heated, Diazomethane emits toxic fumes made of nitrogen oxides; the toxic fumes are also independent of its decomposition. Diazomethane is used after its preparation in ether or in ether that contains traces of ethanol. It is rarely prepared and applied to other solvents which may include dichloromethane. Diazomethane is related to hydrogen cyanide and formaldehyde in its annotation.
Physical and Chemical Properties
Diazomethane has a molecular weight of 42.041 g/mol, and a monoisotopic mass of 42.022 g/mol, which is also its exact mass. Diazomethane has a musty odor, and it is shipped in the form of compressed gas. It has a boiling point of -90 F or -230 C at 760 mm Hg and a melting point of -2290 F or -1450 C.
Diazomethane dissolves in water, and it is highly soluble in dioxane and ether. It has a relative density of 1.45 (water=1) and a relative vapor density 1.45 (air=1).
Copper powder influences the decomposition of diazomethane where nitrogen evolves, and polymethylene’s insoluble white flakes are formed.
Uses
Different sources of media describe the Uses of 334-88-3 differently. You can refer to the following data:
1. It is used as a methylating agent especially for acidic compounds which may include enols, phenols, and carboxylic acids.
2. Powerful methylating agent for acidic Compounds such as carboxylic acids, phenols, enols. For syntheses with diazomethane see the reviews by Smith, Chem. Rev. 23, 193 (1938); Eistert, Z. Angew. Chem. 54, 99, 124 (1941) translated by Spangler in Newer Methods of Preparative Organic Chemistry (New York, 1948) p 513; J. S. Pizey, Synthetic Reagents vol. 2 (John Wiley, New York, 1974) pp 65-142.
3. It is used in organic synthesis as a methylating agent to methylate acidic compoundssuch as carboxylic acids and phenols. Itis used in trace environmental analysis tomethylate chlorophenoxy acid herbicides.
4. Powerful methylating agent for acidic
compounds such as carboxylic acids, phenols,
enols; not manufactured for sale and distribution
because of toxicity and explosivity
Methods of Preparation
Diazomethane can be manufactured from an alkali (potassium carbonate or potassium hydroxide) reaction With N-Nitrosomethyl-P-Toluenesulfonamide. It can also be prepared from ether solutions of diazomethane, where N-nitroso-beta-methylaminoisobutyl methyl ketone in isopropanol and ether is reacted with sodium isopropoxide.
Gaseous diazomethane is prepared from hydrazine and chloroform through a reaction with potassium hydroxide or from nitrosomethylurea and potassium hydroxide.
Precautions
Different sources of media describe the Precautions of 334-88-3 differently. You can refer to the following data:
1. Inhalation, eye or skin contact with diazomethane results in eye irritation, shortness of breath, coughing, headache, chest pains, pulmonary edema and fever.
2. Diazomethane is attractive as a methylating agent for carboxylic acids and phenols because it reacts quickly and highly efficiently with the production of only N2 as a by-product (Black, 1983). Its natural yellow color is discharged as it reacts, providing automatic indication of reaction progress. However, because diazomethane is highly toxic, it should be generated and used only in a well-functioning fume hood. Because it explodes on contact with some metals or ground glass of any type (joints, stoppers, syringes, stopcocks), it should be handled behind a safety shield, and other personal protective equipment should be used. Because it has a boiling point of ?23°C, it is usually handled in the ethereal solutions in which it is generated. Because it explodes on contact with CaSO4, its solutions or vapors must never be dried with drierite. Despite all of these hazards, it can be worked with safely, provided that appropriate precautions are observed.
Chemical Properties
Diazomethane is a flammable, yellow gas or
a liquid under pressure. Musty odor.
Production Methods
Two main methods are used to prepare diazomethane. One uses commercially available apparatus specifically designed for its preparation and distillation while entrained with ether. The resulting ether solution is typically of 0.3–0.4 m concentration and diazomethane is in its purest form. Such apparatus have specialized joints without ground glass and come in a range of sizes for generating diazomethane on scales of around 1, 50, or 300 mmol. The other method uses conventional glassware. Both methods use hydroxide to generate the diazomethane from nitrosamide precursors. The more formal method involves adding N-methyl-N-nitroso-toluenesulfonamide (Fig. 1), also known as Diazald, to KOH. The manufacturer's instructions for the use of this apparatus should be followed explicitly.
Figure 1 Reagents used as precursors to diazomethane.
The home brew method to make diazomethane can be found in its original form in Organic Syntheses (using N-methyl-N-nitrosourea as the precursor) (De Boer and Backer, 1956). This method uses a two-phase system of 50% aqueous KOH and diethyl ether in an Erlenmeyer flask cooled in an ice-water bath and stirred magnetically. The precursor recommended today, because it is safer to store and handle, is the crystalline solid N-methyl-N-nitroso-nitro-guanidine (MNNG). However, MNNG is still considered toxic, a severe irritant, a carcinogen, and a mutagen, and is typically used for generation of diazomethane quantities of 1 mmol. MNNG is slowly added to the two-phase system portion-wise. Sufficient precursor must be used to allow for materials transfer losses of diazomethane that are inevitable in the incomplete separation procedures described following. A yellow color will develop in the ether phase as the diazomethane is generated. After all of the precursor has been added, the solutions may be stirred for 10 min or so to allow the reaction to complete. The upper ether layer is decanted into a clean flask held in an ice-water bath. DO NOT use a separatory funnel with a ground-glass stopcock to separate the aqueous solution from the ether phase. Another portion of ether is added to the reaction flask, and it is stirred at ice-water bath temperature to extract remaining diazomethane. This ether layer is also decanted into the clean flask in the ice-water bath. This process may be repeated. The combined ether phases are likely to contain some dissolved water, which may be removed by adding KOH pellets and allowing the solution to stand in an ice-water bath for 0.5–3 h. The resulting yellow ethereal solution of diazomethane is ready for use. This procedure can be conducted on up to a 60 mmol scale.
Definition
ChEBI: The simplest diazo compound, in which a diazo group is attached to a methylene group.
General Description
Yellow gas with a musty odor. Highly toxic by inhalation Shipped as a liquid under pressure.
Air & Water Reactions
Reacts with water, releasing nitrogen, more stable in ether or dioxane.
Reactivity Profile
Diazomethane undergoes violent thermal decomposition. Above 200°C. the vapors may explode violently if rough glass surfaces are present. Explosions at low temperatures can occur if traces of organic matter are present. [J. Phys. Chem. 35:1403(1931)]. Produces explosions with alkali metals. Reacts with copper powder and to some extent all solid surfaces to produce nitrogen and solid white polymethylene. Reacts with dimethylaminodimethylarsine and trimethyltin in ether with vigorous foaming.
Health Hazard
Different sources of media describe the Health Hazard of 334-88-3 differently. You can refer to the following data:
1. It is a highly toxic gas and an irritant toeye, nose, and the entire respiratory tract.Exposure can cause dizziness, weakness,chest pain, severe headache, fever, asthmaticattack and pneumonia. Exposure to traceconcentrations of this substance can alsoproduce adverse effects, causing coughing,wheezing and headache. There have beenmany reported cases of poisoning. Its toxicitymay be attributed to its strong methylatingproperty.
2. Diazomethane vapor causes severe irritation of the skin, eyes, mucous membranes,
and lungs. It is considered to be a substance with poor warning properties, and the
effects of exposure may be delayed in onset. Symptoms of exposure may include
headache, chest pain, cough, fever, severe asthmatic attacks, and pulmonary edema,
which can be fatal. Exposure of the skin and mucous membranes to diazomethane
may cause serious burns.
Diazomethane is a powerful allergen. Prolonged or repeated exposure to
diazomethane can lead to sensitization of the skin and lungs, in which case asthma-
like symptoms or fever may occur as the result of exposure to concentrations of
diazomethane that previously caused no symptoms. Chronic exposure to
diazomethane has been reported to cause cancer in experimental animals, but this
substance has not been identified as a human carcinogen.
Note that diazomethane is often prepared in situ from precursors that may
themselves be highly toxic and/or carcinogenic.
Fire Hazard
Pure diazomethane gas and liquid are readily flammable and can explode easily. A
variety of conditions have been reported to cause explosions of diazomethane,
including contact with rough surfaces such as ground-glass joints, etched or
scratched flasks, and glass tubing that has not been carefully fire-polished. Direct
sunlight and strong artificial light may also cause explosions of this substance.
Violent reactions may occur on exposure of diazomethane to alkali metals.
Flammability and Explosibility
Pure diazomethane gas and liquid are readily flammable and can explode easily. A variety of conditions have been reported to cause explosions of diazomethane, including contact with rough surfaces such as ground-glass joints, etched or scratched flasks, and glass tubing that has not been carefully fire-polished. Direct sunlight and strong artificial light may also cause explosions of this substance. Violent reactions may occur on exposure of diazomethane to alkali metals.
Safety Profile
Confirmed carcinogen
with experimental tumorigenic data. A
poisonous irritant by inhalation. A powerful
allergen. It can cause pulmonary edema and
frequently causes hypersensitivity leading to
asthmatic symptoms. Mutation data
reported. Highly explosive when shocked,
exposed to heat, or by chemical reaction.
Undiluted liquid or gas may explode on
contact with alkali metals, rough surfaces,
heat (lOO°C), hgh-intensity light, or shock.
When heated to decomposition or on
contact with acid or acid fumes it emits
highly toxic fumes of NOx. Incompatible
with alkali metals; calcium sulfate.
Synthesis
To a solution of potassium hydroxide (30 mL,40%) in ether (100 ml), cooled below 5 °C with ice bath, was added in batches α-nitroso-α-methylurea with stirring. The organic phase was separated and dried over globosity potassium hydroxide for 3 hours. There is diazomethane (~2.6 g) in the ether solution, which was used without further purification.
Potential Exposure
Diazomethane is a powerful methylat-
ing agent for acidic compounds, such as carboxylic acids,
phenols and enols. It is used in pesticide manufacture and
pharmaceutical manufacture.
Carcinogenicity
Diazomethane was administered
to rats and mice by inhalation, dermal, or subcutaneous
injection routes using concentrations of 0.1 or 3.3 mg/mL.
Mice developed lung tumors following either dermal application
or inhalation at both concentrations.
storage
diazomethane should preferably be handled in solution using glassware specially designated for diazomethane (e.g., with Clear-Seal joints) and should be used as soon as possible after preparation. Storage of diazomethane solutions (even at low temperature) is not advisable. All work with diazomethane should be conducted in a fume hood behind a safety shield, and appropriate impermeable gloves, protective clothing, and safety goggles should be worn at all times.
Shipping
UN1953 Compressed gas, toxic, flammable, n.o.s.
Incompatibilities
Heat (at about or above 100
C), shock,
friction, concussion, sunlight, or other intense illuminations
may cause explosions. Contact with alkali metals; drying
agents such as calcium sulfate, or rough edges (such as
ground glass) may cause explosions. Diazo compounds can
detonate. This applies in particular to organic azides that
have been sensitized by the addition of metal salts or strong
acids. Toxic gases are formed by mixing materials of this
class with acids, aldehydes, amides, carbamates, cyanides,
inorganic fluorides, halogenated organics, isocyanates,
ketones, metals, nitrides, peroxides, phenols, epoxides, acyl
halides, and strong oxidizing or reducing agents.
Flammable gases are formed by mixing materials in this
group with alkali metals. Explosive combination can occur
with strong oxidizing agents, metal salts, peroxides, and
sulfides. This chemical is sensitive to prolonged exposure
to heat. This chemical is incompatible with strong
oxidizing agents
.
Waste Disposal
Decompose chemically
with ceric ammonium nitrate under constant agitation and
cooling
.
Check Digit Verification of cas no
The CAS Registry Mumber 334-88-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 334-88:
(5*3)+(4*3)+(3*4)+(2*8)+(1*8)=63
63 % 10 = 3
So 334-88-3 is a valid CAS Registry Number.
InChI:InChI=1/CH2N2/c1-2-3-1/h1H,(H,2,3)
334-88-3Relevant articles and documents
Synthesis of conformationally restricted glutamic acid analogs based on the spiro[3.3]heptane scaffold
Radchenko, Dmytro S.,Grygorenko, Oleksandr O.,Komarov, Igor V.
, p. 2924 - 2930 (2008)
A library of isomeric glutamic acid analogs based on the spiro[3.3]heptane skeleton is designed. Two members of the library, (R)- and (S)-2-amino-spiro[3.3]heptane-2,6-dicarboxylic acid hydrochlorides, were synthesized. The stereochemistry of the synthesi
Scalable On-Demand Production of Purified Diazomethane Suitable for Sensitive Catalytic Reactions
Sheeran, Jillian W.,Campbell, Kiersten,Breen, Christopher P.,Hummel, Gerald,Huang, Changfeng,Datta, Anamika,Boyer, Serge H.,Hecker, Scott J.,Bio, Matthew M.,Fang, Yuan-Qing,Ford, David D.,Russell, M. Grace
supporting information, p. 522 - 528 (2021/02/03)
We have developed a convenient development-scale reactor (0.44 mol/h) to prepare diazomethane from N-methyl-N-nitroso-p-toluenesulfonamide (MNTS) in ～80% yield. Diazomethane (CH2N2) made with this reactor is extracted into nitrogen gas from the liquid reaction mixture, effectively removing it from reagents and byproducts that may interfere in subsequent reactions. Vertically oriented tubular reactors were used to produce and consume diazomethane in situ. Key features of this reactor include high productivity and correspondingly low reactor volume (reactor volume/liquid flow rate = 6.5 min) and a commercially available gas/liquid separator equipped with a selectively permeating hydrophilic membrane. The design of the reactor keeps the inventory below 53 mg of CH2N2 during normal operation. The reactor was demonstrated by generating CH2N2 that was used in a connected continuous reactor. We evaluated esterification reactions and a continuous Pd-catalyzed cyclopropanation reaction with the reactor and achieved high conversion with 1.5 and 4.1 equiv of MNTS precursor, respectively.
Biological evaluation of 3-benzylidenechromanones and their spiropyrazolines-based analogues
Adamus-Grabicka, Angelika A.,Budzisz, Elzbieta,Cieslak, Marcin,Hikisz, Pawe?,Królewska-Golinska, Karolina,Kusz, Joachim,Ma?ecka, Magdalena,Markowicz-Piasecka, Magdalena
, (2020/04/10)
A series of 3-benzylidenechrmanones 1, 3, 5, 7, 9 and their spiropyrazoline analogues 2, 4, 6, 8, 10 were synthesized. X-ray analysis confirms that compounds 2 and 8 crystallize in a monoclinic system in P21/n space groups with one and three molecules in each asymmetric unit. The crystal lattice of the analyzed compounds is enhanced by hydrogen bonds. The primary aim of the study was to evaluate the anti-proliferative potential of 3-benzylidenechromanones and their spiropyrazoline analogues towards four cancer cell lines. Our results indicate that parent compounds 1 and 9 with a phenyl ring at C2 have lower cytotoxic activity against cancer cell lines than their spiropyrazolines analogues. Analysis of IC50 values showed that the compounds 3 and 7 exhibited higher cytotoxic activity against cancer cells, being more active than the reference compound (4-chromanone or quercetin). The results of this study indicate that the incorporation of a pyrazoline ring into the 3-arylideneflavanone results in an improvement of the compounds’ activity and therefore it may be of use in the search of new anticancer agents. Further analysis allowed us to demonstrate the compounds to have a strong inhibitory effect on the cell cycle. For instance, compounds 2, 10 induced 60% of HL-60 cells to be arrested in G2/M phase. Using a DNA-cleavage protection assay we also demonstrated that tested compounds interact with DNA. All compounds at the concentrations corresponding to cytotoxic properties are not toxic towards red blood cells, and do not contribute to hemolysis of RBCs.
