HRID1008618

反应详情

EQUATION

反应方程式

HRID 1008618 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To 6-chloro-1H-indole-2-carbaldehyde (1 equiv.) in DMF at 0° C. was added NaH (1.25 equiv.) portionwise followed by benzhydryl bromide (1.46 equiv.) and Bu4Nl (0.05 equiv.). The mixture was stirred at rt for 42 h before quenching with cold 0.4N HCl at 0° C. After neutralization, the aqueous layer was extracted with ether and the organic layer was washed with cold H2O and dried. Flash chromatography on silica gel gave 1-benzhydryl-6-chloro-1H-indole-2-carbaldehyde in 40% yield.

WORKUP

后处理

  1. custombefore quenching with cold 0.4N HCl at 0° C
  2. extractionAfter neutralization, the aqueous layer was extracted with ether
  3. washthe organic layer was washed with cold H2O
  4. customdried