HRID2304906

反应详情

EQUATION

反应方程式

HRID 2304906 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

At 0° C. 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (2.90 g, 15.29 mmol) was added to a solution of 4-(trifluoromethyl)cyclohexanecarboxylic acid (3.0 g, 15.29 mmol) and 1-hydroxybenzotriazole (2.1 g, 15.29 mmol) in DMF (10 ml) and DCM (10 ml). The reaction mixture was stirred for 20 min at 0° C. A saturated solution of ammonia in methanol (17 ml) was added. The reaction mixture was stirred for 16 hours, while it was warming up to room temperature. It was diluted with ethyl acetate (100 ml) and washed with a 10% aqueous solution of sodium hydrogen sulphate (100 ml). The aqueous phase was extracted with ethyl acetate (2×80 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate (100 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica, using DCM/methanol/25% aqueous ammonia (100:10:1) as eluent, to give 1.99 g of 4-trifluoromethylcyclohexanecarboxylic acid amide.

WORKUP

后处理

  1. customAt 0° C
  2. stirringThe reaction mixture was stirred for 16 hours, while it
  3. temperaturewas warming up to room temperature
  4. washwashed with a 10% aqueous solution of sodium hydrogen sulphate (100 ml)
  5. extractionThe aqueous phase was extracted with ethyl acetate (2×80 ml)
  6. washThe combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate (100 ml)
  7. dry with materialdried over magnesium sulphate
  8. customThe solvent was removed in vacuo
  9. customThe crude product was purified by flash chromatography on silica