Reaktion #1808224

Reaktionsgleichung

2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl) thiazolidine

N-bromosuccinimide

→

2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromothiazoline

Ausbeute 45.3%

Lösungsmittel

chloroform

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturAfter cooling
2. 2
   Waschenthe reaction mixture was washed with an aqueous sodium sulfite solution
3. 3
   Trocknendried over anhydrous magnesium sulfate
4. 4
   SonstigeThe solvent was removed under reduced pressure

Vorschrift

A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl) thiazolidine (1.6 g) and N-bromosuccinimide (2 g) in chloroform (50 ml) was refluxed for 10 hours. After cooling, the reaction mixture was washed with an aqueous sodium sulfite solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.9 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromothiazoline (Compound No. 30).

Quelle