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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236173Generated: October 31, 2026

Chlorosuccinimide → Ethyl 5-chloro-2-phenyloxazole-4-carboxylate

https://huagongshe.com/reaction/2236173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantEthyl 2-phenyl-1,3-oxazole-4-carboxylateHCID 571056—
CatalystSulfuric AcidHCID 1118—
SolventChloroformHCID 6212—
ProductEthyl 5-chloro-2-phenyloxazole-4-carboxylateHCID 6753762337.7%

Reaction Steps

Mixture of 2-phenyl-oxazole-4-carboxylic acid ethyl ester (217 mg, 1 mmol), 1-chloro-pyrrolidine-2,5-dione (400 mg, 3 mmol) and two drops of sulfuric acid in chloroform (10 mL) was heated at 90 degrees for overnight. After the reaction was complete, solvent was evaporated. To the residue, water was added, and then the mixture was extracted with ethyl acetate twice. The organic layers were collected, combined, washed with saturated sodium bicarbonate, dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck silica gel 60, 230-400 mesh, 5-40% ethyl acetate in hexane for 30 min) gave 5-chloro-2-phenyl-oxazole-4-carboxylic acid ethyl ester (95 mg, 37%) as a white solid. LCMS calcd for C12H10ClNO3 (m/e) 251, obsd 252 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714126B2
Source datasetuspto-grants-2010_05
ORD IDord-c38f396e6def4bf5836fc95da9ebe164
Source noteuspto-grants-2010_05