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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride | HCID 57482541 | — |
| Product | Ethyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionate | HCID 57482547 | 83.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888362B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-f55e94b2919340b7b78dc67ff9059a13 |
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| Source note | uspto-grants-2011_02 |
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