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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364259Generated: October 30, 2026

Ethyl Acrylate → Ethyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionate

https://huagongshe.com/reaction/1364259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantSodium HydroxideHCID 14798—
Reactant1-(1-Benzothiophen-4-yl)piperazine hydrochlorideHCID 57482541—
ProductEthyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionateHCID 5748254783.4%

Reaction Steps

5.05 g (19.8 mmol) of 1-Benzo[b]thiophen-4-yl-piperazine hydrochloride was added to an aqueous solution of sodium hydroxide, and the mixture was extracted with methylene chloride. The organic phase was dried over magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in 50 ml of ethanol and ethyl acrylate (2.44 ml, 21.8 mmol) was added thereto, then the reaction mixture was refluxed for 4 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. Isopropyl ether was added to the residue to filter out insoluble matters. The insoluble matters were washed with isopropyl ether and dried to obtain ethyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionate (5.26 g) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888362B2
Source datasetuspto-grants-2011_02
ORD IDord-f55e94b2919340b7b78dc67ff9059a13
Source noteuspto-grants-2011_02