Реакция #1132447

ord-6f76b2409af244a0b486bcafe5621eb8

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe reaction was then stirred for 18 hours at 90° C
  2. 2
    Другоеquenched by the slow addition of ethanol (10 mL)
  3. 3
    КонцентрированиеThe mixture was concentrated
  4. 4
    Экстракцияextracted three times with EtOAc (30 mL)
  5. 5
    ПромывкаThe combined organic extracts were washed with deionized water (20 mL)
  6. 6
    Сушкаdried (MgSO4)
  7. 7
    Фильтрацияfiltered
  8. 8
    Концентрированиеconcentrated
  9. 9
    ДругоеChromatographic 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08568772B2uspto-grants-2013_10