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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161844Generated: October 28, 2026

Ethanol → Ethyl 3-chlorobenzimidate hydrochloride

https://huagongshe.com/reaction/1161844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBenzonitrile, m-chloro-HCID 13015—
ProductEthyl 3-chlorobenzimidate hydrochlorideHCID 21938143100%

Reaction Steps

To a solution of 3-chlorobenzonitrile (50 g, 363 mmol) in anhydrous ethanol (500 mL), cooled to 0° C. in an ice bath, was bubbled HCl (g) through a gas dispersion tube for approximately 20 minutes until the solution was saturated. The resulting reaction mixture was stirred at room temperature for 16 h. Volatiles were removed in vacuo and the residue was triturated with anhydrous ether (˜200 mL). The white solid was collected by filtration and dried in vacuo overnight to afford ethyl 3-chlorobenzimidate hydrochloride (INTERMEDIATE II.1) (80 g, 363 mmol, 100%) which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820649B2
Source datasetuspto-grants-2010_10
ORD IDord-bb4e323615f34b59885f49acecccb010
Source noteuspto-grants-2010_10