HRID568886

反应详情

EQUATION

反应方程式

HRID 568886 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of CuI (20 mg), 1-bromo-6-[(3-butynyl)oxy]hexane (3.04 g), N,N-diethyl-2-iodobenzamide (3.95 g), BTPC (200 mg), N,N-dicyclohexylamine (2.60 g) and acetonitrile (20 ml) was stirred under nitrogen at room temperature for 4.5 h, diluted with ether (200 ml) and filtered. The filtrate was evaporated in vacuo, the residue in ethanol (100 ml) was treated with charcoal and the solvent evaporated in vacuo. The residual oil (5.32 g) in absolute ethanol (190 ml) was hydrogenated over pre-reduced 10% PDO-C (50% paste in water, 1.25 g) in absolute ethanol (20 ml), filtered through hyflo and evaporated in vacuo to give an oil. Purification by FCC eluting with T-EA-triethylamine (95:5:1) followed by FCC eluting with CX-EA (2:1) gave the title compound as a yellow oil (2.04 g). T.l.c. (T-ET-A-40:10:1) Rf 0.14.

WORKUP

后处理

  1. filtrationfiltered
  2. customThe filtrate was evaporated in vacuo
  3. additionthe residue in ethanol (100 ml) was treated with charcoal
  4. customthe solvent evaporated in vacuo
  5. filtrationfiltered through hyflo
  6. customevaporated in vacuo
  7. customto give an oil
  8. customPurification by FCC
  9. washeluting with T-EA-triethylamine (95:5:1)
  10. washeluting with CX-EA (2:1)