Reacción #1556138
ord-78001c445ed240a092fbfd6b97219fc8
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1ConcentraciónThe reaction mixture was concentrated
- 2workup.ADDITIONdiluted with diethyl ether
- 3Lavadowashed twice with saturated aqueous sodium bisulfite
- 4ExtracciónThe aqueous layers were extracted once with diethyl ether
- 5Secadothe combined organic layers were dried over anhydrous sodium sulfate
- 6ConcentraciónThe product was concentrated
- 7Otropurified by flash chromatography (silica gel, 0-50% ethyl acetate/hexanes)
Procedimiento
Methyl 4-amino-3,6-dichloropicolinate (10.0 g, 45.2 millimoles (mmol)), periodic acid (3.93 g, 17.2 mmol), and iodine (11.44 g, 45.1 mmol) were dissolved in methanol (30 mL) and refluxed at 60° C. for 27 h. The reaction mixture was concentrated, diluted with diethyl ether, and washed twice with saturated aqueous sodium bisulfite. The aqueous layers were extracted once with diethyl ether, and the combined organic layers were dried over anhydrous sodium sulfate. The product was concentrated and purified by flash chromatography (silica gel, 0-50% ethyl acetate/hexanes) to provide the title compound as a pale yellow solid (12.44 g, 35.9 mmol, 79%): mp 130.0-131.5° C.; 1H NMR (400 MHz, CDCl3) δ 5.56 (s, 2H), 3.97 (s, 3H); 13C NMR (101 MHz, CDCl3) δ 163.80, 153.00, 152.75, 145.63, 112.12, 83.91, 53.21; EIMS m/z 346.