HRID1045336

反应详情

EQUATION

反应方程式

HRID 1045336 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

1,2-Dilinoleyloxy-3-allyloxypropane (25) (18 g, 28.6 mmol) was dissolved in ethanol (150 mL) in a 500 mL round bottom flask with a stir bar. Trifluoroacetic acid (15 mL) and tetrakis (triphenylphosphine) palladium(0) (5.0 g, 4.3 mmol) were added and the flask flushed with nitrogen. A water condenser was fitted and the flask wrapped tin foil to reduce exposure to light. The reaction was refluxed under nitrogen overnight. The solution was concentrated to an orange oil, then redissolved in DCM (250 mL), and washed with water (2×200 mL) and saturated brine (1×200 mL). The aqueous phases were combined and extracted with DCM (2×100 mL). Organic phases were combined, dried over MgSO4 and concentrated. The crude product was purified by column chromatography to yield 1,2-dilinoleylglycerol as a colorless oil (11.0 g, 18.7 mmol, 65.3%).

WORKUP

后处理

  1. customthe flask flushed with nitrogen
  2. customA water condenser was fitted
  3. temperatureThe reaction was refluxed under nitrogen overnight
  4. concentrationThe solution was concentrated to an orange oil
  5. dissolutionredissolved in DCM (250 mL)
  6. washwashed with water (2×200 mL) and saturated brine (1×200 mL)
  7. extractionextracted with DCM (2×100 mL)
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated
  10. customThe crude product was purified by column chromatography