反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- temperaturethe mixture was refluxed for 1 hour
- customthe magnesium complex prepared
- additionabove added
- customat room temperature
- customovernight
- customThe solvent was removed under reduced pressure
- customthe residue partitioned between ether and 200 ml of 20% ammonium chloride
- washthe organic layer washed with water
- customThe solvent was evaporated under reduced pressure
- customthe residue flash-chromatographed on silica gel
- washeluting with 1% ethyl acetate in heptane