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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712638Generated: November 3, 2026

Benzoyl chloride → HCID 46673126, compound

https://huagongshe.com/reaction/1712638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantEthyl piperazine-1-acetateHCID 207112—
SolventTetrahydrofuranHCID 8028—
ProductHCID 46673126HCID 46673126—

Reaction Steps

1-(Ethoxycarbonylmethyl)piperazine (5.1 g) was dissolved in tetrahydrofuran (300 ml) under a nitrogen atmosphere, and triethylamine (8.25 ml) and benzoyl chloride (3.44 ml) was added thereto with cooling in an ice water bath. The reaction mixture was brought to room temperature, followed by stirring for 4 hours. The reaction mixture was partitioned between ethyl acetate (200 ml) and a saturated aqueous solution of sodium hydrogencarbonate (100 ml). The separated organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (100 ml), water (100 ml) and brine (100 ml), and dried over sodium sulfate. The solvent was distilled off under reduced pressure to give the title compound (8.19 g, quant.) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790885B2
Source datasetuspto-grants-2010_09
ORD IDord-aee5710dc47a40b9b448297e5ea135b8
Source noteuspto-grants-2010_09