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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172088Generated: November 3, 2026

Water → 3-(5-Chloro-1-methyl-3-trifluoromethylpyrazol-4-ylmethanesulfonyl)-5,5-dimethyl-2-isoxazoline

https://huagongshe.com/reaction/1172088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68768624HCID 68768624—
SolventChloroformHCID 6212—
Product3-(5-Chloro-1-methyl-3-trifluoromethylpyrazol-4-ylmethanesulfonyl)-5,5-dimethyl-2-isoxazolineHCID 5900621795.1%

Reaction Steps

16.87 g of m-chloroperbenzoic acid (purity: 70%, 68.4 mmoles) was added, with ice-cooling, to a solution of 8.97 g (27.4 mmoles) of 3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-ylmethylthio)-5,5-dimethyl-2-isoxazoline dissolved in 300 ml of chloroform. The mixture was stirred for 1 hour and then at room temperature over one night to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with chloroform. The resulting organic layer was washed with an aqueous sodium hydrogensulfite solution, an aqueous sodium hydrogencarbonate solution, water and an aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The solid thus obtained was washed with n-hexane to obtain 9.36 g (yield: 95.1%) of 3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-ylmethanesulfonyl)-5,5-dimethyl-2-isoxazoline as white powder (melting point: 115.0 to 116.0° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-b17630a75e784b78aec77c5bf247ec1d
Source noteuspto-grants-2010_11