反应 #1702105

ord-f1e890d60c44408586cd225a88eb3883

反应方程式

CC1=CC[C@@H](C(=O)O)CC1
(1S)-4-Methyl-cyclohex-3-ene-1-carboxylic acid
Cc1ccccc1
toluene
O=C(Cl)C(=O)Cl
oxalyl chloride
CC1=CC[C@@H](C(=O)Cl)CC1
(1S)-4-methyl-cyclohex-3-ene-1-carboxylic acid chloride

反应条件

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

后处理

  1. 1
    温度to warm to ambient temperature
  2. 2
    浓缩The solution was concentrated
  3. 3
    workup.ADDITIONtreated with hexanes
  4. 4
    浓缩concentrated again

实验过程

(1S)-4-Methyl-cyclohex-3-ene-1-carboxylic acid (250 mg, 1.78 mmol), azeotropically dried by evaporation from toluene was dissolved in dichloromethane (4 mL) and treated with dimethylformamide (1 drop). The reaction mixture was cooled to 0° C. and treated dropwise with oxalyl chloride (0.42 mL, 4.5 mmol). The reaction mixture was allowed to warm to ambient temperature while stirring for 4 h. The solution was concentrated, treated with hexanes and concentrated again to afford (1S)-4-methyl-cyclohex-3-ene-1-carboxylic acid chloride as a light yellow oil which was used immediately in the next step.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08765722B2uspto-grants-2014_07