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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801635Generated: October 31, 2026

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

https://huagongshe.com/reaction/1801635

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 numberUS08349840B2
Source datasetuspto-grants-2013_01
ORD IDord-512b13427d8748739d5064a5f457fa8a
Source noteuspto-grants-2013_01