HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376072Generated: October 25, 2026
Benzoyl chloride → Ethyl (1E)-N-benzoylethanimidate
https://huagongshe.com/reaction/1376072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butanamide--hydrogen chloride (1/1) | HCID 22560754 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl (1E)-N-benzoylethanimidate | HCID 13028604 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169929B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-b3d5897404ca48f49df41a273a6d793e |
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| Source note | uspto-grants-2007_01 |
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