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
PROCEDURE
实验过程
In a 50 mL three-neck round-bottomed flask was charged the methyl 4-amino-3,6-dichloro-5-fluoropicolinate (12.1 mmol), toluene (50 mL), and CHCl3 (15 mL). To this suspension was added dropwise a premixed solution of sulfuric acid (0.05 mmol) and acetic anhydride (24.2 mmol), in toluene (5 mL). The reaction mixture was then heated, under a N2 stream, to 55-60° C. and the reaction was monitored by TLC. Once the reaction was deemed complete the heating mantle was removed and the reaction solution was cooled to ambient temperature. The mixture was then added dropwise to a mixture of saturated aqueous NaHCO3/toluene/CHCl3 (180 mL, 3/10/5), stirred for 20 min, and the layers separated using a reparatory funnel. To the organic layer was added silica gel (14.8 g) and the solvent was removed using a rotary evaporator. The crude product on silica was then purified using a Combi-Flash silica gel purification system using ethyl acetate and hexane as eluents. The purity of the product was analyzed by HPLC: mp=183-186° C.; 1H NMR (400 MHz, DMSO-d6) δ 10.5 (s, 1H, NH), 3.93 (s, 3H), 2.17 (s, 3H); 13C NMR (100.6 MHz, DMSO-d6) δ 167.9, 162.8, 151.7, 149.0, 142.8 (d, JF-C=24 Hz), 136.2 (d, JF-C=80 Hz), 134.7 (d, JF-C=56 Hz), 126.6, 53.2, 22.5; 19F NMR (376.5 MHz, DMSO-d6) δ −114.5; MS Calcd. for C9H7Cl2FN2O3: 280.0. Found: 281 (MH+), 245, 180.
WORKUP
后处理
- temperatureThe reaction mixture was then heated, under a N2 stream
- customto 55-60° C.
- customwas removed
- additionThe mixture was then added dropwise to a mixture of saturated aqueous NaHCO3/toluene/CHCl3 (180 mL, 3/10/5)
- customthe layers separated
- additionTo the organic layer was added silica gel (14.8 g)
- customthe solvent was removed
- customa rotary evaporator
- customThe crude product on silica was then purified
- customa Combi-Flash silica gel purification system