HRID1784145

反应详情

EQUATION

反应方程式

HRID 1784145 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

0.35 g (0.62 mmol) N-(3,4-Dimethoxy-phenyl)-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamic acid benzyl ester in 20 mL ethyl acetate and 0.37 mL acetic acid was hydrogenated over Pd/C with atmospheric pressure of H2 for 16 h at room temperature. The catalyst was filtered off and the and the filtrate evaporated to dryness. The acid was used without further purification in the consecutive step. MS(m/e): 488.2 (MH+).

WORKUP

后处理

  1. filtrationThe catalyst was filtered off
  2. customthe and the filtrate evaporated to dryness
  3. customThe acid was used without further purification in the consecutive step