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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261339Generated: October 30, 2026

Water → 3-(1-Chloroethyl)-5-t-butylisoxazole

https://huagongshe.com/reaction/2261339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant1-(5-t-Butyl-isoxazol-3-yl)ethanolHCID 57736312—
SolventPyridineHCID 1049—
Product3-(1-Chloroethyl)-5-t-butylisoxazoleHCID 57736302—

Reaction Steps

1.18 g of 1-(5-t-butyl-isoxazol-3-yl)ethanol was dissolved in 2 ml of pyridine, and 1.36 of 4-toluenesulfonyl chloride was then added under ice-cooling. The mixture was stirred for 5 hours under ice-cooling. After water was added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.60 g of 3-(1-chloroethyl)-5-t-butylisoxazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846956B2
Source datasetuspto-grants-2010_12
ORD IDord-ac395ad5524a47ecbf37e8d382f3a00e
Source noteuspto-grants-2010_12