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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478945Generated: October 25, 2026

Diethyl Pyrocarbonate → 2-(2-t-Butyloxazol-4-yl)-3-chloro-2'-methyl-4'-trifluoromethoxybenzanilide

https://huagongshe.com/reaction/478945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-4-(trifluoromethoxy)anilineHCID 2775546—
Reactant2-(2-t-Butyloxazol-4-yl)-3-chlorobenzoic acidHCID 18003337—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(2-t-Butyloxazol-4-yl)-3-chloro-2'-methyl-4'-trifluoromethoxybenzanilideHCID 1800334128%

Reaction Steps

0.4 Gram of 2-(2-t-butyloxazol-4-yl)-3-chlorobenzoic acid was dissolved in 30 ml of tetrahydrofuran, then 0.3 g of 2-methyl-4-trifluoromethoxyaniline, 0.4 g of DEPC and 0.3 g of triethylamine were added thereto, the resulting mixture was heated under reflux for 3 hours with stirring. After completion of the reaction, the reaction mixture was poured into water, and the objective product was extracted with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, the residue obtained by removal of the solvent by distillation under reduced pressure was purified by the silica gel column chromatography to obtain 0.18 g (yield: 28%) of the objective product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642379B1
Source datasetuspto-grants-2003_11
ORD IDord-3fa1fdeb772e404ba7e0ae4d9264b74c
Source noteuspto-grants-2003_11