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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801636Generated: October 31, 2026

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

https://huagongshe.com/reaction/1801636

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 numberUS08349840B2
Source datasetuspto-grants-2013_01
ORD IDord-bd5ddf950a164300b9f14af17b43b72d
Source noteuspto-grants-2013_01