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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5325Erstellt: 23. Oktober 2026

1,1-Dibromoethane → 2-Imino-3-(3-trifluoromethylphenyl)thiazolidine

https://huagongshe.com/de/reaction/5325

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-DibromoethaneHCID 11201—
EduktPotassium CarbonateHCID 11430—
Edukt3-(Trifluoromethyl)phenylthioureaHCID 735844—
LösungsmittelAcetoneHCID 180—
Produkt2-Imino-3-(3-trifluoromethylphenyl)thiazolidineHCID 22416978110%

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
PatentnummerUS05244863
Quelldatensatzuspto-grants-1993_09
ORD IDord-7abe0b247b3646b18c986acb76de854f
Quellennotizuspto-grants-1993_09