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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907365Generated: October 30, 2026

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

https://huagongshe.com/reaction/1907365

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 numberUS08598162B2
Source datasetuspto-grants-2013_12
ORD IDord-a2054310a9324b3793cdeb8143a4eeea
Source noteuspto-grants-2013_12