反応 #7872
ord-640654338223404497e09faf1387ac75
溶媒
反応条件
後処理
- 1濃縮The mixture was concentrated in vacuo
- 2その他the residue partitioned between EtOAc and H2O
- 3その他the layers separated
- 4抽出extracted with EtOAc
- 5洗浄The combined organic layers were washed with saturated NaHCO3 and brine
- 6乾燥dried over MgSO4
- 7ろ過filtered
- 8濃縮concentrated in vacuo
実験手順
To a stirred solution of 3-aminopyridine (9.41 g, 100 mmol) and triethylamine (16.7 mL, 120 mmol) in CH2Cl2 (300 mL) at 0° C. was added trimethylacetyl chloride (14.8 mL, 120 mmol) dropwise over 15 min. The reaction was warmed to rt and stirred overnight. The mixture was concentrated in vacuo, the residue partitioned between EtOAc and H2O, and the layers separated. The aqueous layer was made basic with saturated NaHCO3 and extracted with EtOAc. The combined organic layers were washed with saturated NaHCO3 and brine, dried over MgSO4, filtered, and concentrated in vacuo to give N-(pyridin-3-yl)-2,2-dimethylpropanamide as a tan solid. 1H NMR (CDCl3, 300 MHz) δ 8.57 (d, 1H), 8.33 (dd, 1H), 8.17 (ddd, 1H), 7.69 (br s, 1H), 7.27 (dd, 1H), 1.33 (s, 9H).