反应 #2329028

ord-8044212375034425a9fa8f3f91130488

反应方程式

Cl
hydrochloric acid
CC(C)(C)c1ccc2c(c1)C(=O)OC2=O
4-t-butylphthalic anhydride
CC(C)(C)c1ccccc1
t-butylbenzene
[Al+3].[Cl-].[Cl-].[Cl-]
Aluminum chloride
CC(C)(C)c1ccc(C(=O)c2cc(C(C)(C)C)ccc2C(=O)O)cc1
benzoic acid
收率 64.0%
CC(C)(C)c1ccc(C(=O)c2cc(C(C)(C)C)ccc2C(=O)O)cc1
4-t-butyl-2-[4-t-butylbenzoyl)benzoic acid
收率 64.0%

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONAdded into a 500 ml three-necked flask under the environment of argon
  2. 2
    workup.ADDITIONAfter the addition, they
  3. 3
    其他After the reaction, ice
  4. 4
    workup.ADDITIONwas added gradually
  5. 5
    过滤After the precipitates were filtered
  6. 6
    洗涤they were thoroughly washed

实验过程

Added into a 500 ml three-necked flask under the environment of argon were 4-t-butylphthalic anhydride 36 g (176 mmole), t-butylbenzene 27 g (200 mmole) and dichloroethane 100 ml. The mixture was cooled to 0° C. Aluminum chloride 56 g (420 mmole) was added gradually to them. After the addition, they were stirred at room temperature overnight. After the reaction, ice was added gradually followed by the addition of concentrated hydrochloric acid. After the precipitates were filtered, they were thoroughly washed to give the benzoic acid substance 32 g (yield 64%, white powder).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07670506B1uspto-grants-2010_03