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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916205Generated: November 1, 2026

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

https://huagongshe.com/reaction/1916205

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 numberUS08618109B2
Source datasetuspto-grants-2013_12
ORD IDord-1077e94f2ff949fdb2e434fb34f8ce94
Source noteuspto-grants-2013_12