Реакция #1121729
ord-b01e6d425e7b4a53aefedf78e63022f2
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1workup.STIRRINGthe reaction was then stirred for 18 hours at 90° C
- 2Другоеquenched by the slow addition of ethanol (10 mL)
- 3КонцентрированиеThe mixture was concentrated
- 4Экстракцияextracted three times with EtOAc (30 mL)
- 5ПромывкаThe combined organic extracts were washed with deionized water (20 mL)
- 6Сушкаdried (MgSO4)
- 7Фильтрацияfiltered
- 8Концентрированиеconcentrated
- 9ДругоеChromatographic purification of the residue (0-5% MeOH in chloroform)
Методика
A toluene (10 mL) solution of 3-(dimethylamino)-1,2-propanediol (98%, 1.00 g, 8.39 mmol, 1.0 equiv)) was carefully added dropwise to a toluene suspension (5 mL) of NaH (60%, 0.34 g, 8.39 mmol, 1.0 equiv) at 0° C. under argon and the resultant was stirred for 15 minutes. A toluene solution (5 mL) of linoleyl methanesulfonate (2.87 g, 8.39 mmol, 1.0 equiv) was added dropwise to the stirring mixture and the reaction was then stirred for 18 hours at 90° C. The mixture was then cooled to room temperature and quenched by the slow addition of ethanol (10 mL). The mixture was concentrated and the residue was taken up with deionized water (20 mL) and extracted three times with EtOAc (30 mL). The combined organic extracts were washed with deionized water (20 mL), dried (MgSO4), filtered, and concentrated. Chromatographic purification of the residue (0-5% MeOH in chloroform) provided 1-(dimethylamino)-4-((9Z,12Z)-octadeca-9,12-dienyloxy)butan-2-ol, a thick, clear oil.