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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582903Generated: October 27, 2026

Potassium Hydroxide → 5-(Chloromethyl)-1,2-oxazole-3-carboxylic acid

https://huagongshe.com/reaction/1582903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 5-chloromethylisoxazole-3-carboxylateHCID 14674306—
SolventEthanolHCID 702—
Product5-(Chloromethyl)-1,2-oxazole-3-carboxylic acidHCID 2186644976.8%

Reaction Conditions

Temperature65 °C

Reaction Steps

14 g (250 mmol) of potassium hydroxide were added to 47.3 g (250 mmol) of ethyl 5-chloromethylisoxazole-3-carboxylate in 150 ml of ethanol, and the reaction mixture was stirred for 6 hours at 60-70° C. After cooling, the mixture was concentrated in vacuo, the residue was taken up in water and extracted with ether, the aqueous phase was acidified with hydrochloric acid and subsequently extracted repeatedly with ether, and the ether phase was dried over sodium sulfate and concentrated in vacuo (oil pump, 50° C.). 31 g of the required product resulted (77% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740647B1
Source datasetuspto-grants-2004_05
ORD IDord-a6726453d7bb47f7847093625a1a8176
Source noteuspto-grants-2004_05