Reaktion #3060

ord-a73c3e09e44447508491ea934b7c975c

Reaktionsgleichung

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

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was warmed to room temperature over 20 minutes
  2. 2
    workup.STIRRINGstirred for 30 minutes
  3. 3
    Sonstigethe organic layer was separated
  4. 4
    WaschenThe organic layer was washed with water (2×100 mL), brine (100 mL)
  5. 5
    Trocknendried over magnesium sulfate
  6. 6
    Einengenconcentrated in vacuo

Vorschrift

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%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731438uspto-grants-1998_03