4-acetylphenoxide

Base Information

• Chemical Name: 4-acetylphenoxide
• CAS No.: 261172-44-5
• Molecular Formula: C₈H₇O₂
• Molecular Weight: 135.142
• Mol file: 261172-44-5.mol

Synonyms:4-acetylphenoxide

Chemical Property of 4-acetylphenoxide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-acetylphenoxide

There total 37 articles about 4-acetylphenoxide 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-acetylphenyl 4-nitrobenzenesulfonate (55660-68-9) → 4-acetylphenoxide (261172-44-5)

Guidance literature:

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

DOI:10.1002/bkcs.10297

Reference yield:

4-acetylphenol radical (54560-34-8) + chlorite (14998-27-7) → 4-acetylphenoxide (261172-44-5) + chlorine dioxide (10049-04-4,25052-55-5)

Guidance literature:

In water; Rate constant; Equilibrium constant; Irradiation;

Reference yield:

4-benzoyloxyacetophenone (1523-18-8) → 4-acetylphenoxide (261172-44-5) + 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

upstream raw materials:

1H-imidazole

1-diethylphosphoryloxy-4-(1-oxoethyl)benzene

4-acetyloxyacetophenone

3-chlorophenoxide

Downstream raw materials:

CH₃COC₆H₄OC(O)Co(CO)4

1H-imidazole

1-diethylphosphoryloxy-4-(1-oxoethyl)benzene

p-Acetylphenyldiphenylphosphat

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.