HRID486278

反应详情

EQUATION

反应方程式

HRID 486278 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of 1-acetoxy-4-dibenzylamino-2-butene (3.0 g, 9.8 mmol) and 2,6-diphenylpiperidine (2.3 g, 9.8 mmol) in THF (25 ml) is treated with tetrakis(triphenylphosphine)palladium (0) (0.5 g, 0.45 mmol) and stirred at room temperature overnight. The reaction mixture is concentrated in vacuo. The residue is redissolved in THF (100 ml) and treated with 20% aqueous sodium hydroxide (25 ml). The mixture is stirred for one hour, concentrated, and extracted with diethyl ether. The ether extracts are dried and concentrated to give an orange oil which is purified by chromatography (silica gel; 5% ethyl acetate in hexanes) to give the title compound in a yield of 2.8 g (59%) as a clear oil. MS m/z 486 (M+)

WORKUP

后处理

  1. concentrationThe reaction mixture is concentrated in vacuo
  2. dissolutionThe residue is redissolved in THF (100 ml)
  3. additiontreated with 20% aqueous sodium hydroxide (25 ml)
  4. stirringThe mixture is stirred for one hour
  5. concentrationconcentrated
  6. extractionextracted with diethyl ether
  7. dry with materialThe ether extracts are dried
  8. concentrationconcentrated
  9. customto give an orange oil which
  10. customis purified by chromatography (silica gel; 5% ethyl acetate in hexanes)