HRID1531270

反应详情

EQUATION

反应方程式

HRID 1531270 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of the title E compound ({5-[(4′-trifluoromethylbiphenyl-2-carbonyl)-amino]indan-2-yl}-carbamic acid tert-butyl ester, 5.19 g, 10.5 mmol) in formic acid (40 mL) is heated to 40° C. with stirring. After 3 h, the reaction mixture is cooled to room temperature and stirring is continued for 16 h. The reaction mixture is concentrated under reduced pressure and the resulting oil dissolved in ethyl acetate. The organic layer is washed with 8% NaHCO3 solution until the aqueous layer remains basic at which point a precipitate forms in the organic layer. The precipitate is collected by filtration to give 4′-trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide. The organic layer of the filtrate is dried (MgSO4) and concentrated under reduced pressure to give a solid. Trituation of the solid with diethyl ether yields additional 4′-trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide.

WORKUP

后处理

  1. stirringstirring
  2. waitis continued for 16 h
  3. concentrationThe reaction mixture is concentrated under reduced pressure
  4. dissolutionthe resulting oil dissolved in ethyl acetate
  5. washThe organic layer is washed with 8% NaHCO3 solution until the aqueous layer
  6. filtrationThe precipitate is collected by filtration