Реакция #578442
ord-b33b965f836d448d8aebd9d35a55d478
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1ДругоеTo a dry 2 L multi-neck round bottom flask fitted with an air stirrer, nitrogen inlet condenser and an additional funnel
- 2workup.ALIQUOTsampled hourly until maximum conversion
- 3ТемператураThe mixture was cooled
- 4Другоеthe organic layer was separated
- 5ЭкстракцияThe aqueous layer was extracted with 3×100 ml of toluene
- 6Сушкаdried over MgSO4
Методика
To a dry 2 L multi-neck round bottom flask fitted with an air stirrer, nitrogen inlet condenser and an additional funnel, 400 ml of THF, 44 g of NaH, and 21.2 g of dihydroethyl linalool were added and heated to 35-40° C. 170 g of dihydrolinalool g was then added to the reaction mixture dropwise over 2 hours. The mixture was aged for 8 hours. 9 g of HMPA (available from Aldrich Chemical Company) was added and the mixture was stirred. 144 g of CH3I was added dropwise to the reaction mixture, further aged for two hours and then sampled hourly until maximum conversion was reached. The mixture was cooled and 800 ml of 5% HCl solution was added, allowed to settle, and the organic layer was separated. The aqueous layer was extracted with 3×100 ml of toluene and then dried over MgSO4 to provide 3-nonene, 7-methoxy-3,7-dimethyl-.