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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-5,5-dimethyl-4,5-dihydro-1,2-oxazole | HCID 11665417 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Isoxazole, 4,5-dihydro-5,5-dimethyl-3-[(phenylmethyl)thio]- | HCID 12137651 | 62.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06841519B1 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-00ebf6a41ae44654a9f2430f70939c63 |
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| Source note | uspto-grants-2005_01 |
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