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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376072Generated: October 25, 2026

Benzoyl chloride → Ethyl (1E)-N-benzoylethanimidate

https://huagongshe.com/reaction/1376072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantButanamide--hydrogen chloride (1/1)HCID 22560754—
SolventDichloromethaneHCID 6344—
ProductEthyl (1E)-N-benzoylethanimidateHCID 1302860486%

Reaction Steps

Ethylacetamidate hydrochloride 1.0 g (8.09 mmol) was dissolved in dichloromethane 40 ml at room temperature, added dropwise triethylamine 1.08 ml (16.99 mmol) and stirred for 30 minutes at room temperature. Then, the reacting solution was cooled to 0° C., benzoylchloride 1.03 g (7.35 mmol) was slowly added dropwise in the reacting solution for 10 minutes and stirred for 4 hours at room temperature. After completing the reaction, the reacting solution was washed with water and saturated brine, and then dried with anhydrous magnesium sulfate. Then, the resulting product was filtered under reduced pressure and purified through a flash column chromatography (ethyl acetate:normal hexane=2:8). As a result, N-(1-ethoxy-ethylidene)-benzamide (1.20 g, yield: 86%) was obtained as a liquid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169929B2
Source datasetuspto-grants-2007_01
ORD IDord-b3d5897404ca48f49df41a273a6d793e
Source noteuspto-grants-2007_01