Reacción #1876816
ord-587fa6dd1dba43fda10d118c83fddfdf
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe reaction mixture was then removed from ice
- 2workup.ADDITIONUpon the addition of 10% hydrochloric acid (84 mL)
- 3Extracciónextracted with ethyl acetate
- 4Secadodried with magnesium sulfate
- 5Concentraciónconcentrated
- 6OtroPurification by column chromatography (25% ethyl acetate/heptane)
Procedimiento
2-Chloro-4-phenylquinoline was prepared by the following method (Rxn-1). 2-Aminobenzophenone (21 g, 106.5 mmol) was dissolved in methylene chloride (213 mL) and triethylamine (22.3 mL, 159.8 mmol) was added slowly. After cooling to 0° C., acetylchloride (8.3 mL, 117.2 mmol) was added to the reaction mixture dropwise. The reaction mixture was then removed from ice and allowed to stir overnight. Upon the addition of 10% hydrochloric acid (84 mL), the aqueous layers were combined and extracted with ethyl acetate. The organic phases were combined, dried with magnesium sulfate, and concentrated. Purification by column chromatography (25% ethyl acetate/heptane) gave 2-acetamidobenzophenone.