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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187522Generated: October 25, 2026

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

https://huagongshe.com/reaction/1187522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
SolventTolueneHCID 1140—
ProductEthyl (1E)-N-benzoylethanimidateHCID 1302860482%

Reaction Steps

First, 15.5 g of ethyl acetimidate hydrochloride, 150 mL of toluene, and 31.9 g of triethylamine (Et3N) were put into a 500-mL three-neck flask and stirred at room temperature for 10 minutes. With a 50-mL dropping funnel, a mixed solution of 17.7 g of benzoyl chloride and 30 mL of toluene were added dropwise to this mixture, and the mixture was stirred at room temperature for 24 hours. After a predetermined time elapsed, the reaction mixture was suction-filtered, and the solid was washed with toluene. The obtained filtrate was concentrated to give N-(1-ethoxyethylidene)benzamide (a red oily substance, 82% yield). A scheme of the synthesis of Step 1 is shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673459B2
Source datasetuspto-grants-2014_03
ORD IDord-58c95e2905544d7eb7dd114ddac66ddc
Source noteuspto-grants-2014_03