Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655638Generated: October 31, 2026

Tetrahydrofuran → 3-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)propanol

https://huagongshe.com/reaction/655638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionateHCID 57482547—
SolventWaterHCID 962—
Product3-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)propanolHCID 574825485%

Reaction Steps

Lithium aluminum hydride (1.18 g, 24.8 mmol) was added to a solution of 5.26 g (16.5 mmol) of ethyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionate in a tetrahydrofuran (THF) solution (55 ml) under ice cooling, and the mixture was stirred at room temperature for 4 hours. To the reaction solution, water (1.2 ml), 15% aqueous sodium hydroxide solution (1.2 ml), and water (3.6 ml) were added in this order and the mixture was stirred at room temperature. Insoluble matter was removed by filtration, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:2→ethyl acetate) and concentrated to dryness under reduced pressure to obtain 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propan-1-ol (0.23 g) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071600B2
Source datasetuspto-grants-2011_12
ORD IDord-703fbf2958744f0ea467833afb1d0b3b
Source noteuspto-grants-2011_12