تفاعل #1005952
ord-24945c868ee545f8bff1fe7849701947
معادلة التفاعل
Ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate
3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)pyrrolidine
potassium carbonate
→
title compound
المردود 86.5%
ethyl 2-[3-(3,4,5-trichlorophenyl)-3-(trifluoro-methyl)pyrrolidin-1-yl]-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate
المردود 86.5%
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةAfter cooling
- 2استخلاصextracted with ethyl acetate
- 3تجفيفThe organic layer was dried over magnesium sulfate
- 4أخرىThe solvent was evaporated off under reduced pressure
- 5أخرىthe residue was then purified by a silica gel chromatography
الإجراء التجريبي
Ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate (1.4 g) [see J. Het. Chem., 22, 1621 (1985)], 3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)pyrrolidine (1.7 g), and potassium carbonate (0.8 g) were added to N,N-dimethylformamide (50 mL), followed by heating at 100° C. for five hours. After cooling, the reaction solution was poured over ice water, and then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, and the residue was then purified by a silica gel chromatography to obtain the title compound (2.5 g, 86%).