反应 #3060

ord-a73c3e09e44447508491ea934b7c975c

反应方程式

O=C(Br)CBr
bromoacetyl bromide
COc1ccc(N)cc1
4-methoxyaniline
CCN(C(C)C)C(C)C
diisopropylethylamine
COc1ccc(NC(=O)CBr)cc1
title compound
COc1ccc(NC(=O)CBr)cc1
Bromo-N-(4-methoxyphenyl)acetamide

反应条件

温度
-20°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction mixture was warmed to room temperature over 20 minutes
  2. 2
    workup.STIRRINGstirred for 30 minutes
  3. 3
    其他the organic layer was separated
  4. 4
    洗涤The organic layer was washed with water (2×100 mL), brine (100 mL)
  5. 5
    干燥dried over magnesium sulfate
  6. 6
    浓缩concentrated in vacuo

实验过程

The title compound was prepared via a modification of the literature procedure (Vloon, W. J.; Kruk, C.; Pandit, U. K.; Hofs, H. P.; McVie, J. G. J. Med Chem. 1987, 30, 20-4.). To a solution of 4-methoxyaniline (4.93 g, 40.0 mmol) in methylene chloride (200 mL) was added diisopropylethylamine (7.66 mL, 44.0 mmol). The resulting mixture was cooled to -20° C., and bromoacetyl bromide (3.82 mL, 44.0 mmol) was added slowly. The reaction mixture was warmed to room temperature over 20 minutes and stirred additional 30 minutes. The reaction mixture was diluted with water (100 mL), stirred for 30 minutes and the organic layer was separated. The organic layer was washed with water (2×100 mL), brine (100 mL), dried over magnesium sulfate and concentrated in vacuo to afford a beige solid (9.68 g) which was recrystallized from ethyl acetate to provide bromo-N-(4'-methoxyphenyl)acetamide as a whim crystal (6.31 g, 65%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05731438uspto-grants-1998_03