HRID372923

反应详情

EQUATION

反应方程式

HRID 372923 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
3 °C

PROCEDURE

实验过程

A grignard reagent solution prepared from 1.53 g of magnesium, 10.5 g of 1-bromo-4-fluorobenzene and 70 ml of tetrahydrofuran was added dropwise at 3°-7° C. within 45 minutes to a mixture of 16.9 g of crude 2-chloro-5-[(tetrahydro-2-pyranyloxy)methyl]pyridine, 60 ml of tetrahydrofuran and 0.62 g of 1,3-bis(diphenylphosphino)-propanenickel-(II) chloride. The dark reaction mixture was stirred at 3° C. for a further 1 hr. and at room temperature for 2 hrs. and then extracted with 200 ml of diethyl ether and 120 ml of 0.5N ammonium chloride solution. The organic phase was washed neutral with water, dried over sodium sulphate, filtered and concentrated. Chromatographic purification of the residue on 230 g of silica gel with hexane/ethyl acetate (vol. 9:1) yielded 13.4 g of 2-(4-fluorophenyl)-5-[(tetra-hydro-2-pyranyloxy)methyl]pyridine as a yellowish oil.

WORKUP

后处理

  1. customThe dark reaction mixture
  2. waitand at room temperature for 2 hrs
  3. extractionand then extracted with 200 ml of diethyl ether and 120 ml of 0.5N ammonium chloride solution
  4. washThe organic phase was washed neutral with water
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customChromatographic purification of the residue on 230 g of silica gel with hexane/ethyl acetate (vol. 9:1)