HRID1843285

反应详情

EQUATION

反应方程式

HRID 1843285 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
35 °C

PROCEDURE

实验过程

A mixture of 1-benzyl-1,2,3,4-tetrahydroquinolin-7-ol (824 mg, 3.44 mM) and triethylamine (0.6 mL) in dry tetrahydrofuran (THF, 5 ml) was stirred for half an hour under nitrogen atmosphere at room temperature (35° C.). To the stirred reaction mixture, p-tolyl isocyanate (651 mg/ml, 5.16 mM) was added at once and then the reaction mixture was further stirred for 72 hours under N2 atmosphere at RT. The reaction mixture was concentrated under vacuum and then was quenched with distilled water followed by the extraction with chloroform (3×15 mL). The combined fractions of chloroform was again washed with water and dried over sodium sulphate. Further concentration of chloroform fraction under vacuum afforded the crude product, which was finally crystallized with methanol-ether (1:5) to give 8b as solid. Yield: 1.023 g, 79.77%.

WORKUP

后处理

  1. additionwas added at once and then the reaction mixture
  2. stirringwas further stirred for 72 hours under N2 atmosphere at RT
  3. concentrationThe reaction mixture was concentrated under vacuum
  4. customwas quenched with distilled water
  5. extractionfollowed by the extraction with chloroform (3×15 mL)
  6. washThe combined fractions of chloroform was again washed with water
  7. dry with materialdried over sodium sulphate
  8. customFurther concentration of chloroform fraction under vacuum afforded the crude product, which
  9. customwas finally crystallized with methanol-ether (1:5)