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HRID 478945作成日:2026年10月25日

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

https://huagongshe.com/reaction/478945

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl PyrocarbonateHCID 3051—
反応物TriethylamineHCID 8471—
反応物2-Methyl-4-(trifluoromethoxy)anilineHCID 2775546—
反応物2-(2-t-Butyloxazol-4-yl)-3-chlorobenzoic acidHCID 18003337—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-(2-t-Butyloxazol-4-yl)-3-chloro-2'-methyl-4'-trifluoromethoxybenzanilideHCID 1800334128%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06642379B1
出典データセットuspto-grants-2003_11
ORD IDord-3fa1fdeb772e404ba7e0ae4d9264b74c
出典メモuspto-grants-2003_11