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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744104Generated: October 26, 2026

Pyridine → 2,2,2-Trichloroethyl 4-bromo-5-methylisoxazol-3-ylcarbamate

https://huagongshe.com/reaction/1744104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-5-methyl-1,2-oxazol-3-amineHCID 2774464—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2,2,2-Trichloroethyl 4-bromo-5-methylisoxazol-3-ylcarbamateHCID 22235755—

Reaction Steps

To a mixture of 3-amino-4-bromo-5-methylisoxazole (2.58 g, 14.6 mmol) and DMAP (893 mg, 7.3 mmol) in 60 mL dichloromethane at −78° C. was added pyridine (6 ml, 74.1 mmol) followed by 2,2,2-trichloroethyl chloroformate (8 ml, 58 mmol). The reaction was allowed to warm to room temperature while stirring over ca. 4 hours. Ice water was added, the aqueous phase neutralized with saturated aq. NaHCO3, and the product extracted with ether (3×), dried over Na2SO4 and concentrated in vacuo. The crude product was purified by flash chromatography (20% ethyl acetate/hexane) to afford 2,2,2-trichloroethyl 4-bromo-5-methylisoxazol-3-ylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012075B2
Source datasetuspto-grants-2006_03
ORD IDord-5c84ee7143104145afdca445389f7a2d
Source noteuspto-grants-2006_03