HRID1255580
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 93 °C
PROCEDURE
实验过程
2,6-Dichloro-3-(trifluoromethyl)pyridine (5.00 g, 23.2 mmol) and 28% aqueous ammonia (150 mL) were placed in a 250 mL autoclave. The mixture was heated at 93° C. for 21 h. The reaction was cooled to rt and extracted with EtOAc (100 mL×3). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated under vacuum to give the crude product, which was purified by column chromatography on silica gel (2-20% EtOAc in petroleum ether as eluant) to give 6-chloro-5-(trifluoromethyl)pyridin-2-amine (2.1 g, 46% yield). 1H NMR (400 MHz, DMSO-d6) δ 7.69 (d, J=8.4 Hz, 1H), 7.13 (br s, 2H), 6.43 (d, J=8.4 Hz, 1H). MS (ESI) m/z (M+H)+197.2
WORKUP
后处理
- temperatureThe reaction was cooled to rt
- extractionextracted with EtOAc (100 mL×3)
- dry with materialThe combined organic extracts were dried over anhydrous Na2SO4
- customevaporated under vacuum
- customto give the crude product, which
- customwas purified by column chromatography on silica gel (2-20% EtOAc in petroleum ether as eluant)