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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952846Generated: October 27, 2026

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

https://huagongshe.com/reaction/1952846

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

47.3 g (250 mmol) of ethyl 5-chloromethylisoxazole-3-carboxylate in 150 ml of ethanol were mixed with 14 g (250 mmol) of potassium hydroxide, and the mixture was stirred at 60-70° C. for 6 h. After cooling and concentration under reduced pressure, the residue was taken up in water and extracted with ether, the aqueous phase was acidified with hydrochloric acid and then extracted several times with ether, and the ether phase was dried over sodium sulfate and concentrated under reduced pressure (oil pump, 50° C.). 31 g of the required product were obtained (77% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114358
Source datasetuspto-grants-2000_09
ORD IDord-f240dec859874514930a0cecc8b078e3
Source noteuspto-grants-2000_09