4-formylphenoxide ion

Base Information

• Chemical Name: 4-formylphenoxide ion
• CAS No.: 18938-17-5
• Molecular Formula: C₇H₅O₂
• Molecular Weight: 121.115
• Mol file: 18938-17-5.mol

Synonyms:4-formylphenoxide ion

Chemical Property of 4-formylphenoxide ion

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-formylphenoxide ion

There total 34 articles about 4-formylphenoxide ion which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

4-formylphenyl 4-nitrobenzenesulfonate (55660-69-0) → 4-formylphenoxide ion (18938-17-5)

Guidance literature:

With sodium hydroxide; In water; dimethyl sulfoxide; acetonitrile; at 25 ℃; Kinetics;

DOI:10.1002/bkcs.10297

Reference yield:

4-formylphenyl benzoate (5339-06-0) → 4-formylphenoxide ion (18938-17-5) + benzoic acid (65-85-0,8013-63-6)

Guidance literature:

With hydroxide; In water; dimethyl sulfoxide; at 25 ℃; Kinetics; Alkaline hydrolysis;

DOI:10.1021/jo026339g

Reference yield:

piperidine (110-89-4) + 4-formylphenyl benzoate (5339-06-0) → N-benzoylpiperidine (776-75-0) + 4-formylphenoxide ion (18938-17-5)

Guidance literature:

In water; dimethyl sulfoxide; at 25 ℃; Kinetics;

DOI:10.1021/jo0606958

upstream raw materials:

1H-imidazole

4-((diethoxyphosphoryl)oxy) benzaldehyde

4-formylphenyl acetate

3-chlorophenoxide

Downstream raw materials:

p-nitrophenolate

4-formylphenyl diphenyl phosphate

4-formylphenyl acetate

2-Nitrophenolate ion

Refernces

• 1、 Um, Ik-Hwan,Park, Kyoung-Ho. "Kinetic Study on Nucleophilic Substitution Reactions of O-Phenyl O-Y-substituted-Phenyl Thionocarbonates with 1,8-Diazabicyclo[5.4.0]undec-7-ene in Acetonitrile". . p. 1169 - 1173. Retrieved 2017/09/13.
• 2、 Kim, Myung-Joo,Kim, Min-Young,Um, Ik-Hwan. "Kinetic study on alkaline hydrolysis of Y-substituted phenyl picolinates: Effects of modification of nonleaving group from benzoyl to picolinyl on reactivity and reaction mechanism". . p. 1138 - 1142. Retrieved 2015/07/15.