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
284 mg (4.34 mmol) of electrolytic zinc is put into suspension under an argon atmosphere, to which 0.033 ml of 1-2 dibromoethane and 1 ml of tetrahydrofuran are added. After stirring for 3 minutes at 60° C. the reaction medium is left to return to ambient temperature. 0.047 ml of trimethylsilyl chloride is added and stirring is carried out for 30 minutes at ambient temperature. 1 g (3.2 mmol) of 2 solubilized beforehand in 2 ml of tetrahydrofuran is added. This reaction mixture is stirred for 45 minutes at ambient temperature and it is added to a solution containing 30 mg (0.032 mmol) of tris(dibenzylideneacetone) dipalladium marketed by Aldrich and 30 mg (0.13 mmol) of tris(2-furyl)phosphine marketed by LANCASTER. Then 1 g (4 mmol) of 3 solubilized beforehand in 10 ml of tetrahydrofuran is added. The reaction mixture is left under magnetic stirring at 60° C. for 2 hours, then left to return to ambient temperature, filtered on clarcel and extracted between ethyl acetate and a saturated aqueous solution of sodium bicarbonate. After extracting the aqueous phase twice with ethyl acetate, the organic phases are combined and dried over magnesium sulphate. The ethyl acetate is evaporated off under reduced pressure (2 kPa) and the crude residue is purified by chromatography on silicagel eluting with a heptane/ethyl acetate mixture 4:1. 350 mg (yield=30%) of expected product is recovered in the form of a yellow oil.
WORKUP
后处理
- additionare added
- waitis left
- customto return to ambient temperature
- stirringstirring
- waitis carried out for 30 minutes at ambient temperature
- stirringThis reaction mixture is stirred for 45 minutes at ambient temperature
- additionit is added to a solution
- waitThe reaction mixture is left
- stirringunder magnetic stirring at 60° C. for 2 hours
- waitleft
- customto return to ambient temperature
- filtrationfiltered on clarcel
- extractionextracted between ethyl acetate
- extractionAfter extracting the aqueous phase twice with ethyl acetate
- dry with materialdried over magnesium sulphate
- customThe ethyl acetate is evaporated off under reduced pressure (2 kPa)
- customthe crude residue is purified by chromatography on silicagel
- washeluting with a heptane/ethyl acetate mixture 4:1