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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235888Generated: November 3, 2026

4-Chlorobenzoyl chloride → 4-Chloro-N-[2-(furan-2-yl)-2-oxoethyl]benzamide

https://huagongshe.com/reaction/235888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-1-(furan-2-yl)ethan-1-one--hydrogen chloride (1/1)HCID 13226138—
SolventWaterHCID 962—
Product4-Chloro-N-[2-(furan-2-yl)-2-oxoethyl]benzamideHCID 1336142898.2%

Reaction Steps

To a mixture of 10 g of (2-furylcarbonyl)methylamine hydrochloride, 12.5 g of sodium bicarbonate, 200 ml of ethyl acetate and 100 ml of water are dropwise added 12.0 g of 4-chlorobenzoyl chloride at a temperature below 10° C. under stirring. The mixture is stirred at room temperature for 3 hours. Then, the ethyl acetate layer is collected, washed with water and dried. Said ethyl acetate layer is evaporated under reduced pressure to remove solvent. 16.0 g of N-(4-chlorobenzoyl)-(2-furylcabonyl)methylamine are thereby obtained. Yield: 98.2%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642313
Source datasetuspto-grants-1987_02
ORD IDord-4a359727c8094b9190ab91730f2d13e8
Source noteuspto-grants-1987_02