Реакция #6649

ord-6b77fd970be54f8dbe3fb67395b6565b

Уравнение реакции

CCCCCC
hexane
CC(C)=CC(=O)Cl
3,3-dimethylacryloyl chloride
Nc1ccc(Br)cc1
4-bromoaniline
CC(C)=CC(=O)Nc1ccc(Br)cc1
title compound
CC(C)=CC(=O)Nc1ccc(Br)cc1
N-(4-Bromophenyl)3,3-dimethylacrylamide

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe organic layer was separated
  2. 2
    Экстракцияthe aqueous layer was extracted with 2×50 ml of hexanes
  3. 3
    Промывкаwashed successively with 30 ml of water and 2×30 ml of saturated NaCl solution
  4. 4
    Сушкаdried (MgSO4)
  5. 5
    ДругоеThe solvent was removed in vacuo
  6. 6
    Другоеthe residue purified by recrystallization from an ethyl acetate and hexanes mixture

Методика

To a solution of 9.48 g (80 mmol) of 3,3-dimethylacryloyl chloride in 200 ml of dry THF was added with vigorous shaking a solution of 13.76 g (80 mmol) of 4-bromoaniline in 300 ml of dry THF. The mixture was stood at room temperature for 2 h and then treated with 80 g of ice followed by 200 ml of hexane. The organic layer was separated and the aqueous layer was extracted with 2×50 ml of hexanes. The organic layers were combined and washed successively with 30 ml of water and 2×30 ml of saturated NaCl solution and then dried (MgSO4). The solvent was removed in vacuo and the residue purified by recrystallization from an ethyl acetate and hexanes mixture to give the title compound as colorless crystals. PMR (CDCl3): δ 1.91 (3H, s), 2.23 (3H, s), 5.73 (1H, broad s), 7.38-7.55 (5H, m).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05248777uspto-grants-1993_09