Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172076Generated: October 31, 2026

Water → HCID 17862855, compound

https://huagongshe.com/reaction/1172076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 17862867HCID 17862867—
SolventChloroformHCID 6212—
ProductHCID 17862855HCID 1786285576.4%

Reaction Steps

2.1 g of m-chloroperbenzoic acid (purity: 70%, 12.2 mmoles) was added, with ice-cooling, to a solution of 0.9 g of 3-(5-cyano-1-methyl-3-trifluoromethyl-1H-pyrazol-4-ylmethylthio)-5,5-dimethyl-2-isoxazoline (crude compound) dissolved in 50 ml of chloroform. The mixture was stirred for 1 hour and then at room temperature for 12 hours to give rise to a reaction. After confirmation of 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 resulting solid was washed with n-hexane to obtain 0.43 g (yield: 76.4%) of 3-(5-cyano-1-methyl-3-trifluoromethyl-1H-pyrazol-4-ylmethylsulfonyl)-5,5-dimethyl-2-isoxazoline as a white powder (melting point: 105.0 to 108.0° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-cd08fb9febdc4e87a3452d63970740fd
Source noteuspto-grants-2010_11