反应详情

温度

65 °C

2-(4-fluoro-3-nitrophenyl)-1,3-benzoxazole (200 mg, 0.77 mmol) was dissolved in DMSO (5 mL) and K2CO3 (267 mg, 1.94 mmol) was added. The resulting yellow mixture was warmed to 65° C. and tert-butylcyanoacetate (137 mg, 0.97 mmol) was added dropwise. The dark red mixture was heated to 65° C. for 30 min, cooled to rt, and poured into H2O. The aqueous layer was acidified to pH 3 (with a 10% aqueous HCl solution) and it was extracted with EtOAc (3×). The organics were combined, washed with brine (2×), dried over Na2SO4, and evaporated to dryness. The yellow residue and p-toluenesulfonic acid (29.5 mg, 0.15 mmol) were dissolved in toluene (15 mL) and the mixture was refluxed for 20 h. After cooling to rt, the mixture was poured in H2O and the two layers were separated. The aqueous was extracted with EtOAc (3×), the organics were combined, dried over Na2SO4, and evaporated to dryness. Purification of the residue by flash chromatography on silica gel eluting with EtOAc:hexanes (3:7 to 2:3 to 1:1) afforded the desired [4-(1,3-benzoxazol-2-yl)-2-nitrophenyl]acetonitrile as an orange solid (M.p. 203° C.). 1H NMR (CDCl3, 300 MHz) δ 8.79 (s, 1H), 8.57 (dd, 1H), 7.97 (d, 1H), 7.86 (m, 2H), 7.54–7.44 (m, 2H), 4.50 (s, 2H). MS (ESI) 280 (M+H)+.

1. temperatureThe dark red mixture was heated to 65° C. for 30 min
2. temperaturecooled to rt
3. extractionwas extracted with EtOAc (3×)
4. washwashed with brine (2×)
5. dry with materialdried over Na2SO4
6. customevaporated to dryness
7. temperaturethe mixture was refluxed for 20 h
8. temperatureAfter cooling to rt
9. customthe two layers were separated
10. extractionThe aqueous was extracted with EtOAc (3×)
11. dry with materialdried over Na2SO4
12. customevaporated to dryness
13. customPurification of the residue by flash chromatography on silica gel eluting with EtOAc:hexanes (3:7 to 2:3 to 1:1)