Реакция #578442

ord-b33b965f836d448d8aebd9d35a55d478

Уравнение реакции

Реагенты

Нет

Растворители

Условия реакции

Температура
37.5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеTo a dry 2 L multi-neck round bottom flask fitted with an air stirrer, nitrogen inlet condenser and an additional funnel
  2. 2
    workup.ALIQUOTsampled hourly until maximum conversion
  3. 3
    ТемператураThe mixture was cooled
  4. 4
    Другоеthe organic layer was separated
  5. 5
    ЭкстракцияThe aqueous layer was extracted with 3×100 ml of toluene
  6. 6
    Сушкаdried 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-.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07531489B2uspto-grants-2009_05