Réaction #3060

ord-a73c3e09e44447508491ea934b7c975c

Équation de réaction

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

Conditions de réaction

Température
-20°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture was warmed to room temperature over 20 minutes
  2. 2
    workup.STIRRINGstirred for 30 minutes
  3. 3
    Autrethe organic layer was separated
  4. 4
    LavageThe organic layer was washed with water (2×100 mL), brine (100 mL)
  5. 5
    Séchagedried over magnesium sulfate
  6. 6
    Concentrationconcentrated in vacuo

Mode opératoire

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%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05731438uspto-grants-1998_03