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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655639Generated: November 1, 2026

Water → 4-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)butyl acetate

https://huagongshe.com/reaction/655639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Butanol, 4-bromo-, 1-acetateHCID 78491—
Reactant1-(1-Benzothiophen-4-yl)piperazine hydrochlorideHCID 57482541—
SolventDimethylformamideHCID 6228—
Product4-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)butyl acetateHCID 5748254955.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

1.0 g (3.9 mmol) of 1-benzo[b]thiophen-4-yl-piperazine hydrochloride was suspended in 20 ml of dimethylformamide (DMF), and potassium carbonate (1.3 g, 9.4 mmol) and 4-bromobutyl acetate (0.7 ml, 4.8 mmol) were added thereto. The reaction mixture was stirred at 80° C. for 6 hours, cooled to room temperature, and water was added thereto, and extracted with ethyl acetate. The organic phase was washed with water, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (dichloromethane:methanol=30:1), and concentrated to dryness under reduced pressure to obtain 4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl acetate (0.72 g) as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071600B2
Source datasetuspto-grants-2011_12
ORD IDord-d0b9ca50fbfc4892821483abf8a60284
Source noteuspto-grants-2011_12