反应 #2314283

ord-e3313ea46cd7402aa009ca69600977fe

反应方程式

Cl
HCl
CC(C)=CCCC1=CCC(CC(=O)Cl)CC1
acid chloride
CC(C)=CCCC1=CCC(CC(=O)Cl)CC1
(4-(4-Methyl-3-pentenyl)-3-cyclohexenyl)acetyl chloride
COc1ccccc1
anisole
COc1ccc(C(=O)CC2CC=C(CCC=C(C)C)CC2)cc1
4-Methoxyphenyl (4-(4-methyl-3-pentenyl)-3-cyclohexenyl)methyl ketone

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooled in an ice/ethanol bath
  2. 2
    workup.STIRRINGstirred for 30 minutes
  3. 3
    萃取The aqueous layer is extracted with dichloromethane
  4. 4
    洗涤the combined organic layers are sequentially washed with water, sodium bicarbonate, and water
  5. 5
    干燥dried over magnesium sulfate
  6. 6
    浓缩The solution is concentrated in vacuo

实验过程

A solution of acid chloride 2C (R=4-Methyl-3-pentenyl) (10 g) in anhydrous dichloromethane (100 mL) is added dropwise to a mixture of ferric chloride (7.8 g) and anisole 2D (4.5 g) in dichloromethane (175 mL), cooled in an ice/ethanol bath. The resulting mixture is gradually warmed to room temperature and stirred overnight. The mixture is poured into 25% HCl (150 mL) and stirred for 30 minutes. The aqueous layer is extracted with dichloromethane, and the combined organic layers are sequentially washed with water, sodium bicarbonate, and water, then dried over magnesium sulfate. The solution is concentrated in vacuo.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06413448B1uspto-grants-2002_07