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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760146Generated: October 29, 2026

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

https://huagongshe.com/reaction/1760146

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

To a solution of 2.8 g (22.5 mmoles) of benzylmercaptan dissolved in 50 ml of dimethylformamide were added, in a nitrogen current, 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. 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, and 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 (refractive index nD20=1.5521).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06841519B1
Source datasetuspto-grants-2005_01
ORD IDord-00ebf6a41ae44654a9f2430f70939c63
Source noteuspto-grants-2005_01