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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760147Generated: October 30, 2026

Potassium Carbonate → Isoxazole, 3-[[(2,6-difluorophenyl)methyl]thio]-4,5-dihydro-5,5-dimethyl-

https://huagongshe.com/reaction/1760147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Methylsulfonyl-5,5-dimethyl-2-isoxazolineHCID 12137656—
ReactantHCID 22597338HCID 22597338—
ReactantSodium Formaldehyde SulfoxylateHCID 23689980—
ReactantSodium hydrogen sulfide hydrateHCID 53442613—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductIsoxazole, 3-[[(2,6-difluorophenyl)methyl]thio]-4,5-dihydro-5,5-dimethyl-HCID 1213765580.5%

Reaction Steps

To a solution of 5.0 g (28.2 mmoles) of 3-methylsulfonyl-5,5-dimethyl-2-isoxazoline (present compound No. 2-1) dissolved in 50 ml of DMF were added, with ice-cooling, 4.5 g (purity: 70%, 56.1 mmoles) of sodium hydrogensulfide hydrate, 7.8 g (56.4 mmoles) of potassium carbonate and 8.7 g (56.5 mmoles) of Rongalit. The mixture was stirred for 2 hours. Thereto was added 5.8 g (28.0 mmoles) of 2,6-difluorobenzylbenzyl bromide. The mixture was stirred at room temperature for 12 hours to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic phase was washed with 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 (solvent system=hexane-ethyl acetate) to obtain 5.8 g (yield: 80.0%) of 3-(2,6-difluorobenzylthio)-5,5-dimethyl-2-isoxazoline as a white powder (melting point: 77 to 80° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06841519B1
Source datasetuspto-grants-2005_01
ORD IDord-59c9adbd69be439aa9beb7ada96991da
Source noteuspto-grants-2005_01