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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172082Generated: October 25, 2026

Potassium Carbonate → [(5-Chloro-3-methyl-isothiazol-4-yl)methylthio]-5,5-dimethyl-2-isoxazoline

https://huagongshe.com/reaction/1172082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium hydrosulfideHCID 28015—
Reactant3-Methylsulfonyl-5,5-dimethyl-2-isoxazolineHCID 12137656—
Reactant4-Chloromethyl-5-chloro-3-methylisothiazoleHCID 17862905—
ReactantSodium Formaldehyde SulfoxylateHCID 23689980—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[(5-Chloro-3-methyl-isothiazol-4-yl)methylthio]-5,5-dimethyl-2-isoxazolineHCID 1786290399.7%

Reaction Steps

0.82 g of sodium hydrosulfide (purity: 70%, 10.00 mmoles) was added at the room temperature to a solution of 0.89 g (5.00 mmoles) of 5,5-dimethyl-3-methylsulfonyl-2-isoxazoline dissolved in 10 ml of N,N-dimethylformamide. The mixture was stirred for 2 hours. Thereto were added 0.70 g (5.00 mmoles) of anhydrous potassium carbonate, 0.78 g (5.00 mmoles) of Rongalit and 0.91 g (5.00 mmoles) of 5-chloro-4-chloromethyl-3-methylisothiazole. The resulting mixture was stirred at room temperature overnight 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 ethyl acetate. The resulting organic layer was washed with water and an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography to obtain 1.38 g (yield: quantitative) of [(5-chloro-3-methyl-isothiazol-4-yl)-methylthio]-5,5-dimethyl-2-isoxazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-a8464246aa3c4a7aab5610ca99e7d079
Source noteuspto-grants-2010_11