Реакция #46458
ord-c9bb23be4d014b61b2df65620189bc16
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ДругоеThe DMF was removed under vacuum, and 1M HCl
- 2workup.ADDITIONwas added until the residue
- 3ЭкстракцияThe mixture was extracted with ethyl acetate
- 4Сушкаthe combined organic phase was dried over magnesium sulfate
- 5Фильтрацияfiltered
- 6Концентрированиеconcentrated under reduced pressure
Методика
2-Bromo-4-methyl-6-iodophenol (7.82 gm, 25 mmol) and cinnamyl bromide (4.93 g, 25 mmol) were added to DMF (20 ml). Diisopropylethylamine (5.3 ml, 30.4 mmol) was added and the mixture heated to 60° C. for 15 minutes and then allowed stir for 16 hours at room temperature. The DMF was removed under vacuum, and 1M HCl was added until the residue was acidic. The mixture was extracted with ethyl acetate, and the combined organic phase was dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give 1-bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzene (10.86 g, 100% yield).