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
PROCEDURE
实验过程
1,1-Bis(2-methoxyphenyl)ethene (15.6 g), toluene (35 ml) and anisole (35 ml) were combined in a flask and 35 ml of a 3.7M hexane solution of Red-Al was added. The mixture was heated to reflux with stirring whereupon it turned dark red. After 2 hours the heat was removed and the mixture was allowed to stir overnight. The excess hydride reagent was carefully quenched with 1.0N hydrochloric acid. The mixture was then diluted with ether and the ethereal solution separated, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain a golden-brown oil. This was triturated with hexane to obtain 3.70 of the title compound. The proton and carbon NMR spectra were consistent with the assigned structure.
WORKUP
后处理
- temperatureThe mixture was heated
- temperatureto reflux
- customAfter 2 hours the heat was removed
- stirringto stir overnight
- customThe excess hydride reagent was carefully quenched with 1.0N hydrochloric acid
- additionThe mixture was then diluted with ether
- customthe ethereal solution separated
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated by evaporation under reduced pressure
- customto obtain a golden-brown oil
- customThis was triturated with hexane