Реакция #457499

ord-6b610ebf91754880a244f3c223e634ad

Реагенты

Нет

Растворители

Условия реакции

Температура
100°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеTo a flask fitted with a condenser and nitrogen inlet
  2. 2
    ТемператураAfter cooling to room temperature
  3. 3
    Другоеthe reaction was quenched with water (1000 mL)
  4. 4
    ДругоеThe phases were separated
  5. 5
    Экстракцияthe aqueous phase was extracted with ethyl acetate (3×400 mL)
  6. 6
    СушкаAfter drying the organic phases over MgSO4
  7. 7
    Фильтрацияfiltering
  8. 8
    Концентрированиеconcentrating in vacuo

Методика

To a flask fitted with a condenser and nitrogen inlet was added 3,4-epoxytetrahydrofuran (20 g, 0.23 mol), isobutyronitrile (100 ml, 5 vol), benzyl alcohol (124 g, 1.15 mol, 5 eq.) and finally magnesium perchlorate (10.3 g, 0.046 mol, 0.2 eq). The solution was heated at 100° C. for 24 hours. After cooling to room temperature, the reaction was quenched with water (1000 mL). The phases were separated and the aqueous phase was extracted with ethyl acetate (3×400 mL). After drying the organic phases over MgSO4, filtering and concentrating in vacuo, the trans-3-benzyloxy-4-hydroxytetrahydrofuran was isolated by column chromatography to give 29 g (66% yield) of a clear colorless liquid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06140516uspto-grants-2000_10