反应 #93504

ord-01834e72521f43caa6f799cf0744450a

反应方程式

[Cl-].[NH4+]
ammonium chloride
[Li][CH2]CCC
butyl lithium
C#Cc1ccc(Cl)cc1
1-chloro-4-ethynylbenzene
C1CO1
ethylene oxide
OCCC#Cc1ccc(Cl)cc1
title compound
OCCC#Cc1ccc(Cl)cc1
4-(4-Chlorophenyl)-3-butyn-1-ol

溶剂

反应条件

温度
-78°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他to cold reaction mixture
  2. 2
    温度to warm to room temperature for 2 hours
  3. 3
    温度cool to -78° C.
  4. 4
    温度to warm to room temperature
  5. 5
    其他Monitor progress of reaction with thin-layer chromatography on silica gel (methylene chloride)
  6. 6
    workup.WAITAfter 18 hours
  7. 7
    萃取extract with 150 ml diethyl ether
  8. 8
    过滤Dry organic layer with magnesium sulfate and then filter
  9. 9
    其他evaporate solvent

实验过程

Dissolve 14.2 g (0.104 mole) of 1-chloro-4-ethynylbenzene in 35 ml dry THF and cool to -78° C. Add 49 ml butyl lithium to cold reaction mixture and allow to warm to room temperature for 2 hours. After 2 hours, cool to -78° C. and then add 5.8 ml (0.114 mole) ethylene oxide in 20 ml THF. Allow to warm to room temperature. Monitor progress of reaction with thin-layer chromatography on silica gel (methylene chloride). After 18 hours, add 150 ml saturated aqueous ammonium chloride solution and extract with 150 ml diethyl ether. Wash organic layer with 2×100 ml saturated aqueous sodium chloride solution. Dry organic layer with magnesium sulfate and then filter, and evaporate solvent to obtain the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04613609uspto-grants-1986_09