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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22040Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/22040

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktButyl chloroformateHCID 61140—
Edukt2-Imino-3-(3-trifluoromethylphenyl)thiazolidineHCID 22416978—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Butoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidineHCID 5421249340,5%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05426188
Quelldatensatzuspto-grants-1995_06
ORD IDord-4655013adc7c40efa849fa31ccac77fb
Quellennotizuspto-grants-1995_06