Реакция #1876816
ord-587fa6dd1dba43fda10d118c83fddfdf
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ДругоеThe reaction mixture was then removed from ice
- 2workup.ADDITIONUpon the addition of 10% hydrochloric acid (84 mL)
- 3Экстракцияextracted with ethyl acetate
- 4Сушкаdried with magnesium sulfate
- 5Концентрированиеconcentrated
- 6ДругоеPurification by column chromatography (25% ethyl acetate/heptane)
Методика
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.