HRID22259

反应详情

EQUATION

反应方程式

HRID 22259 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-60 °C

PROCEDURE

实验过程

A solution of p-bromotoluene (13.5 g) in 50 ml of tetrahydrofuran was added to magnesium (1.5 g) and 1 crystal of iodine in a little tetrahydrofuran, and the mixture was refluxed for 1 hour. In a separate flask, a solution of 2,3-lutidine (6.5 g) in 100 ml of tetrahydrofuran was cooled to about -60° C., and the magnesium complex prepared above added, followed by phenyl chloroformate (8 ml). The mixture was stirred for 1 hour at -60° C., then at room temperature overnight. The solvent was removed under reduced pressure, the residue partitioned between ether and 200 ml of 20% ammonium chloride, the organic layer washed with water, followed by dilute hydrochloric acid. The solvent was evaporated under reduced pressure, and the residue flash-chromatographed on silica gel, eluting with 1% ethyl acetate in heptane, to yield 12.4 g of 1,6-dihydro-2,3-dimethyl-6-(4-methylphenyl)-1-phenoxycarbonyl pyridine, m.p. 106° C.

WORKUP

后处理

  1. temperaturethe mixture was refluxed for 1 hour
  2. customthe magnesium complex prepared
  3. additionabove added
  4. customat room temperature
  5. customovernight
  6. customThe solvent was removed under reduced pressure
  7. customthe residue partitioned between ether and 200 ml of 20% ammonium chloride
  8. washthe organic layer washed with water
  9. customThe solvent was evaporated under reduced pressure
  10. customthe residue flash-chromatographed on silica gel
  11. washeluting with 1% ethyl acetate in heptane