تفاعل #607398

معادلة التفاعل

3-(4-nitrophenyl)-1H-1,2,4-triazole

1-bromo-4-(trifluoromethyl)benzene

cesium carbonate

8-hydroxyquinoline

→

title compound

المردود 63.0%

3-(4-nitrophenyl)-1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazole

المردود 63.0%

المذيبات

N,N′-dimethylformamide water

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةThe reaction was cooled to room temperature (about 22° C.)
2. 2
   أخرىquenched with ammonium hydroxide (10 mL)
3. 3
   استخلاصThe reaction mixture was extracted with ethyl acetate
4. 4
   أخرىThe organic layer was separated
5. 5
   غسيلwashed with water (3×100 mL) and brine (300 mL)
6. 6
   أخرىThe organic layer was separated
7. 7
   تجفيفdried over sodium sulfate
8. 8
   ترشيحfiltered
9. 9
   تركيزconcentrated
10. 10
    أخرىPurification by flash column chromatography (silica gel)

الإجراء التجريبي

A mixture of 3-(4-nitrophenyl)-1H-1,2,4-triazole (20.0 g, 105 mmol), 1-bromo-4-(trifluoromethyl)benzene (28.0 g, 124 mmol), cesium carbonate (68.4 g, 210 mmol), copper(I) iodide (2.59 g, 13.6 mmol), and 8-hydroxyquinoline (1.80 g, 12.4 mmol) in N,N′-dimethylformamide/water (9:1, 142 mL) under nitrogen was heated to 140° C. for 18 hours. The reaction was cooled to room temperature (about 22° C.) and quenched with ammonium hydroxide (10 mL). The reaction mixture was extracted with ethyl acetate. The organic layer was separated and washed with water (3×100 mL) and brine (300 mL). The organic layer was separated and dried over sodium sulfate, filtered, and concentrated. Purification by flash column chromatography (silica gel) using 0-65% ethyl acetate/petroleum ether as eluent provided the title compound as a white solid (22.0 g, 63%): 1H NMR (300 MHz, CDCl3) δ 8.72 (s, 1H), 8.42-8.34 (m, 4H), 7.94 (d, J=8.7 Hz, 2H), 7.84 (d, J=8.5 Hz, 2H); ESIMS m/z 335 ([M+H]+).

المصدر