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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801638Generated: October 31, 2026

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

https://huagongshe.com/reaction/1801638

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 methylene chloride, and carbon tetrachloride (30 ml) and triphenyl phosphine (4.06 g, 15.5 mmol) were added thereto followed by stirring under reflux for 3 hours. The reaction mixture was cooled to room temperature, then methanol and methylene chloride were added thereto so as to make the mixture uniform. Silica gel (30 g) was added to the uniform solution, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (silica gel: 300 g, n-hexane:ethyl acetate=2:1), then 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 numberUS08349840B2
Source datasetuspto-grants-2013_01
ORD IDord-20fdbbda4f044b4d86abb178ace889da
Source noteuspto-grants-2013_01