Reacción #57787
ord-435f973cdb9d4431b3d43eeefb9a3641
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Temperaturarefluxed for 1 h
- 2workup.STIRRINGThe reaction mixture was stirred overnight at rt
- 3Extracciónthe resulting mixture extracted with ethyl acetate (2×150 ml)
- 4SecadoThe combined organic layers were dried over Na2SO4
- 5OtroAfter removal of solvent
- 6Otrothe residue was purified by the flash chromatography
- 7OtroCrystallization of the product from Et2O/hexane mixture
Procedimiento
To a solution of nBuLi (0.0730 mol) in hexane was added N-methyl imidazole (0.0608 mol) drop wise at -40° C. over 30 min under a nitrogen atmosphere. The resulting yellow solution was stirred for a further 3 hr at rt, and then refluxed for 1 h. 2-amino-5-chlorobenzoic acid (1.74 g, 0.01014 mole) in dry ether (60 ml) was then added to the reaction mixture. The reaction mixture was stirred overnight at rt. To the reaction mixture was added saturated NH4Cl solution and the resulting mixture extracted with ethyl acetate (2×150 ml). The combined organic layers were dried over Na2SO4. After removal of solvent, the residue was purified by the flash chromatography using ethyl acetate/hexane (1:4) as eluent. Crystallization of the product from Et2O/hexane mixture gave 300 mg (13.7%) of product as yellow solid.