反应 #1303

ord-3c9f9ed9d7a3470fad54d7ea759b23b8

反应方程式

O=C(O)Cc1ccc(Br)cc1
4-bromophenylacetic acid
O=S(=O)(O)O
H2SO4
CCO
ethanol
O=C([O-])[O-].[K+].[K+]
K2CO3
CCOC(=O)Cc1ccc(Br)cc1
title compound
CCOC(=O)Cc1ccc(Br)cc1
Ethyl (4-bromophenyl)acetate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤filtered
  2. 2
    浓缩The filtrate was concentrated in vacuo
  3. 3
    workup.ADDITIONdiluted with Et2O (200 ml)
  4. 4
    洗涤washed with 10% aqueous NaHCO3 (10 ml) and brine (10 ml)
  5. 5
    干燥dried over MgSO4
  6. 6
    浓缩concentrated in vacuo

实验过程

A solution of 43 g (200 mmol) of 4-bromophenylacetic acid and 0.2 g of conc. H2SO4 in 470 ml of ethanol was refluxed for 16 hours. The reaction mixture was cooled to ambient temperature, stirred with 6 g of solid K2CO3 for 30 minutes and then filtered. The filtrate was concentrated in vacuo, diluted with Et2O (200 ml), washed with 10% aqueous NaHCO3 (10 ml) and brine (10 ml), dried over MgSO4 and concentrated in vacuo to give the title compound as a colorless oil.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723620uspto-grants-1998_03