反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 120 °C
PROCEDURE
实验过程
To a solution of 5-bromo-2-chloro-4-methylpyridine (5.0 g, 20 mmol) in N,N-dimethylformamide (38 mL) was added tert-butoxybis(dimethylamino)methane (7.0 mL, 33.9 mmol). The reaction mixture was heated at 120° C. for 2 hours. The cooled reaction mixture was concentrated in vacuo to afford a thick orange oil, which was redissolved in tetrahydrofuran (40 mL) and slowly poured into a separate flask containing slurry of sodium periodate in water (150 mL) at 0° C. The reaction flask was equipped with an overhead stirrer and allowed to warm to room temperature. The reaction mixture was mixed vigorously for three hours, and then diluted with dichloromethane (150 mL) and filtered. The collected solids were washed with dichloromethane (2×150 mL), and the organic layer was separated from the filtrate and washed with saturated sodium bicarbonate solution (50 mL). The aqueous layer was neutralized via addition of solid sodium bicarbonate, and then back-extracted with dichloromethane (100 mL). The organic portions were combined, dried over sodium sulfate, filtered, and evaporated in vacuo to afford a residue that was purified by flash chromatography (silica, 120 g, ISCO, 0-40% ethyl acetate in heptane) to afford the title compound as an off-white solid (4.03 g, 80%). 1H NMR (500 MHz, d6-DMSO) δ 10.10 (s, 1H), 8.85 (s, 1H), 7.81 (s, 1H).
WORKUP
后处理
- customThe cooled reaction mixture
- concentrationwas concentrated in vacuo
- customto afford a thick orange oil, which
- additionslowly poured into a separate flask
- customThe reaction flask was equipped with an overhead stirrer
- temperatureto warm to room temperature
- additionThe reaction mixture was mixed vigorously for three hours
- filtrationfiltered
- washThe collected solids were washed with dichloromethane (2×150 mL)
- customthe organic layer was separated from the filtrate
- washwashed with saturated sodium bicarbonate solution (50 mL)
- additionThe aqueous layer was neutralized via addition of solid sodium bicarbonate
- extractionback-extracted with dichloromethane (100 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated in vacuo
- customto afford a residue that
- customwas purified by flash chromatography (silica, 120 g, ISCO, 0-40% ethyl acetate in heptane)