Реакция #84034
ord-7e3b810e270a4f29aefca102ad63e1a8
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ФильтрацияThe reaction mixture was filtrated
- 2Другоеthe solvent was removed in vacuum
- 3workup.DISSOLUTIONThe obtained residue was dissolved in ethyl acetate (1.2 L)
- 4Промывкаwashed with water
- 5ДругоеThe organic layer was separated
- 6Сушкаdried over sodium sulphate
- 7Фильтрацияfiltrated
- 8Концентрированиеconcentrated
Методика
2,2-dibromo-1-(6-bromonaphthalen-2-yl)ethanone (90.0 g, 221 mmol, 1.00) was dissolved in tetrahydrofurane (800 mL), triethylamine (27.67 mL, 199 mmol, 0.9 equiv.) was added followed by diethyl phosphite (45.8 g, 332 mmol, 1.50 equiv.). The reaction mixture was stirred overnight. The reaction mixture was filtrated and the solvent was removed in vacuum. The obtained residue was dissolved in ethyl acetate (1.2 L) and washed with water. The organic layer was separated, dried over sodium sulphate, filtrated and concentrated to yield crude 2-bromo-1-(6-bromonaphthalen-2-yl)ethanone (70.3 g). Recrystallization from acetonitrile gave 30 g (first batch) and 6.5 g (second batch) of 2-bromo-1-(6-bromonaphthalen-2-yl)ethanone (50%)