HRID1790905

反应详情

EQUATION

反应方程式

HRID 1790905 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

A mixture of 5-bromoindole-2-carboxylic acid ethyl ester (2.68 g, 10 mmol), tert-butyl acrylate (4.4 mL, 30 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.7 g, 1 mmol) and triethylamine (17 mL) in acetic acid (17 mL) was heated at 120° C. in a closed vessel for 6 hrs. The cooled reaction mixture was poured into water and dichloromethane. The biphasic mixture was filtered through a pad of celite and the aqueous layer was extracted with dichloromethane (2×). The combined organic layers were washed with saturated sodium bicarbonate solution, brine, dried and concentrated. The residue was purified by column chromatography (10% of ethyl acetate in hexanes) to give 900 mg (28%) of 5-(2-tert-butoxycarbonyl-vinyl)-1H-indole-2-carboxylic acid ethyl ester.

WORKUP

后处理

  1. customThe cooled reaction mixture
  2. filtrationThe biphasic mixture was filtered through a pad of celite
  3. extractionthe aqueous layer was extracted with dichloromethane (2×)
  4. washThe combined organic layers were washed with saturated sodium bicarbonate solution, brine
  5. customdried
  6. concentrationconcentrated
  7. customThe residue was purified by column chromatography (10% of ethyl acetate in hexanes)