Реакция #1929031
ord-c08a5405d5904f36a6efde542595a009
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ТемператураThe reaction mixture was then heated
- 2Температураto reflux for 5 hours
- 3workup.WAITIt was then left
- 4ЭкстракцияThe organic phase was extracted with ethyl acetate
- 5Сушкаdried with sodium sulfate
- 6ДругоеThe combined organic phase was evaporated to dryness and 100 mL of 30% ethyl acetate in hexane
- 7workup.ADDITIONwas added to the solid
- 8workup.STIRRINGwith stirring at room temperature for 8 hours
- 9ФильтрацияThe suspension was filtered
- 10Промывкаthe solids were washed with hexane
- 11Другоеdried
- 12Другоеyielding 2 of white solids as the product which
Методика
4.0 g (17.3 mmol) of dibenzoselenophene and 150 mL of dry ether were added in a 250 mL three necked flask under nitrogen. To the mixture, 11.5 mL of BuLi (1.6 M in hexane) was added slowly at room temperature. The reaction mixture was then heated to reflux for 5 hours. The reaction mixture was cooled to −78° C. and 5 mL of trimethyl borate was added. It was then left to stir at room temperature for overnight. About 50 mL of 1 M HCl was added to the reaction mixture. The organic phase was extracted with ethyl acetate and dried with sodium sulfate. The combined organic phase was evaporated to dryness and 100 mL of 30% ethyl acetate in hexane was added to the solid with stirring at room temperature for 8 hours. The suspension was filtered, the solids were washed with hexane and dried, yielding 2 of white solids as the product which was confirmed by NMR