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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354044Generated: October 27, 2026

Phosgene → (3-tert-Butyl-isoxazol-5-yl)-thiocarbamic acid S-(4-methoxy-phenyl)ester

https://huagongshe.com/reaction/2354044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantPotassium CarbonateHCID 11430—
Reactant4-MethoxybenzenethiolHCID 12765—
Reactant3-Tert-butyl-1,2-oxazol-5-amineHCID 2095694—
SolventTetrahydrofuranHCID 8028—
Product(3-tert-Butyl-isoxazol-5-yl)-thiocarbamic acid S-(4-methoxy-phenyl)esterHCID 59380989—

Reaction Steps

A mixture of 4-Methoxy-benzenethiol (0.20 g, 1 eq) and potassium carbonate (0.47 g, 2.5 eq) in dry THF was allowed to stir at room temperature under argon for an hour. Then the stirred suspension was cooled to 0° C. and to it was added drop wise a solution of phosgene (0.17 g 1.2 eq). The reaction stirred at 0° C. for half an hour. Then 3-tert-Butyl-isoxazol-5-ylamine (0.20 g, 1 eq) in THF was added dropwise. The reaction was allowed to warm to room temperature and stirred overnight. The solvent was removed and extracted with ethyl acetate and water. The organic layer was dried over magnesium sulfate and solvent removed. It was purified by HPLC. Yield: 157 mg (36%), LC/MS [MH+] 307.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750160B2
Source datasetuspto-grants-2010_07
ORD IDord-b6478700b8df4881af4b891e4c08a6d0
Source noteuspto-grants-2010_07