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HRID 22040作成日:2026年10月25日

Triethylamine → 2-Butoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine

https://huagongshe.com/reaction/22040

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Butyl chloroformateHCID 61140—
反応物2-Imino-3-(3-trifluoromethylphenyl)thiazolidineHCID 22416978—
溶媒TetrahydrofuranHCID 8028—
生成物2-Butoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidineHCID 5421249340.5%

反応手順

A solution of N-(3-trifluoromethylphenyl)thiourea (6.1 g) , dibromoethane (5.7 g) and anhydrous potassium carbonate (11.5 g) in acetone (60 ml) was refluxed for 1 day. The solvent was removed by distillation therefrom, and the residue was extracted with ethyl ether, washed with water, dried over anhydrous magnesium sulfate and subjected to column chromatography to give 7.5 g of 2-imino-3-(3-trifluoromethylphenyl)thiazolidine. The thus obtained 2-imino-3- (3-trifluoromethylphenyl) thiazolidine (1.0 g), n-butyl chlorocarbonate (0.61 g) and triethylamine (1.2 g) were dissolved in tetrahydrofuran, and the resultant solution was stirred at room temperature for 5 hours. The solvent was removed, and the residue was extracted with ethyl acetate, washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 0.57 g of 2-butoxycarbonylimino-3- (3-trifluoromethylphenyl) thiazolidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426188
出典データセットuspto-grants-1995_06
ORD IDord-4655013adc7c40efa849fa31ccac77fb
出典メモuspto-grants-1995_06