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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22040생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/22040

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Butyl chloroformateHCID 61140—
반응물2-Imino-3-(3-trifluoromethylphenyl)thiazolidineHCID 22416978—
용매TetrahydrofuranHCID 8028—
생성물2-Butoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidineHCID 5421249340.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05426188
출처 데이터셋uspto-grants-1995_06
ORD IDord-4655013adc7c40efa849fa31ccac77fb
출처 메모uspto-grants-1995_06