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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292782Generated: October 31, 2026

Water → Isoxazole, 4,5-dihydro-5,5-dimethyl-3-[(phenylmethyl)thio]-

https://huagongshe.com/reaction/1292782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl mercaptanHCID 7509—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-5,5-dimethyl-4,5-dihydro-1,2-oxazoleHCID 11665417—
SolventDimethylformamideHCID 6228—
ProductIsoxazole, 4,5-dihydro-5,5-dimethyl-3-[(phenylmethyl)thio]-HCID 1213765162.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

3.2 g (23.2 mmoles) of anhydrous potassium carbonate and 3.0 g (22.5 mmoles) of 3-chloro-5,5-dimethyl-2-isoxazoline were added, in a nitrogen atmosphere, to a solution of 2.8 g (22.5 mmoles) of benzylmercaptan dissolved in 50 ml of N,N-dimethylformamide. The mixture was stirred at 100° C. for 2 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 layer was washed with 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 residue was purified by silica gel column chromatography to obtain 3.1 g (yield: 62.0%) of 3-benzylthio-5,5-dimethyl-2-isoxazoline as a yellow oily substance (nD20=1.5521).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238689B2
Source datasetuspto-grants-2007_07
ORD IDord-a79a02ce764b4eca8252993771fcff75
Source noteuspto-grants-2007_07