HRID655641

反应详情

EQUATION

反应方程式

HRID 655641 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

3.56 g (12.9 mmol) of 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propan-1-ol was suspended in 30 ml of dichloromethane, and carbon tetrachloride (30 ml) and triphenyl phosphine (4.06 g, 15.5 mmol) were added thereto. The mixture was refluxed with heating for 3 hours. The reaction solution was cooled to room temperature, then methanol and dichloromethane were added thereto to homogenize the mixture. Silica gel (30 g) was added to the solution, and the solvent was evaporated under reduced pressure. The obtained residue was loaded on silica gel column (300 g) and extracted with a solvent mixture of n-hexane:ethyl acetate=2:1. The extraction solution was concentrated under reduced pressure to obtain 1-benzo[b]thiophen-4-yl-4-(3-chloropropyl)piperazine (2.36 g) as colorless oil.

WORKUP

后处理

  1. temperatureThe mixture was refluxed
  2. temperaturewith heating for 3 hours
  3. additionSilica gel (30 g) was added to the solution
  4. customthe solvent was evaporated under reduced pressure
  5. extractionextracted with a solvent mixture of n-hexane
  6. concentrationThe extraction solution was concentrated under reduced pressure