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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655641Generated: October 29, 2026

Methanol → 1-Benzo[b]thiophen-4-yl-4-(3-chloropropyl)piperazine

https://huagongshe.com/reaction/655641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCarbon TetrachlorideHCID 5943—
ReactantTriphenylphosphineHCID 11776—
Reactant3-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)propanolHCID 57482548—
SolventDichloromethaneHCID 6344—
Product1-Benzo[b]thiophen-4-yl-4-(3-chloropropyl)piperazineHCID 57482551—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071600B2
Source datasetuspto-grants-2011_12
ORD IDord-52edf86f6148474bb4651c8effb6e48a
Source noteuspto-grants-2011_12