Reacción #535341
ord-5f91dae6a2a64518914e109f7d9e558a
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ExtracciónThe aqueous solution was extracted with benzene twice
- 2Lavadothe combined benzene solution was washed with 10% NaOH solution
- 3Secadodried with Na2SO4
- 4Concentraciónconcentrated
- 5OtroSilica gel chromatography (EtOAc:Hexanes=5:95) gave product
- 6workup.ADDITIONstill containing a few percentage of the other regioisomer
- 7OtroIt was recrystallized with EtOAc/Hexanes
Procedimiento
To 1-methylnaphthalene (8.0 g, 56 mmol) in round bottom flask at 0° C. was added nitric acid (26 mL) dropwise. (NOTE: A slow addition of nitric acid is most important to avoid the formation of the other regioisomers). After the reaction mixture was stirred for an additional 15 min at 0° C., it was poured into 65 mL of H2O. The aqueous solution was extracted with benzene twice and the combined benzene solution was washed with 10% NaOH solution, dried with Na2SO4, and concentrated. Silica gel chromatography (EtOAc:Hexanes=5:95) gave product still containing a few percentage of the other regioisomer. It was recrystallized with EtOAc/Hexanes to give 9.0 g (43%) of 1.