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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500554Generated: October 30, 2026

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

https://huagongshe.com/reaction/1500554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionateHCID 57482547—
SolventTetrahydrofuranHCID 8028—
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 tetrahydrofuran (55 ml) with cooling in an ice-bath, followed by stirring at room temperature for 4 hours. Water (1.2 ml), 15% sodium hydroxide aqueous solution (1.2 ml), and water (3.6 ml) were added to the reaction mixture in this order with stirring at room temperature. Insoluble matters were removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:2→ethyl acetate), then concentrated and dried under reduced pressure to obtain 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propane-1-ol (0.23 g) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206167B2
Source datasetuspto-grants-2015_12
ORD IDord-3aefa2bf87b14e90ba6659421f522c04
Source noteuspto-grants-2015_12