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芍药酮的溴化反应 被引量:4

Study on Bromination of paeonol
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摘要 The bromination of paeonol with bromine and copper(Ⅱ)bromide was studied.The target compounds were different because of the different solvents.When paeonol was brominated with reagents like bromine in anhydrous diethyl ether and anhydrous aluminium trichloride,5bromo4methoxy2hydroxyacetophenone was obtained.The yield was 445%.Like cupric bromide in chloroformethyl acetate and anhydrous ethanol,the yield we obtained ωbromo4methoxy5bromo2hydroxyacetophenone was 475%.Paeonol was selectively brominated by copper(Ⅱ)bromide in anhydrous methanol(or chloroformethyl acetate)to give ωbromo4methoxy2hydroxyacetophenone in yield of 633%(or 487%).The structures of the target compounds were characterized by IR,1H NMR and MS. The bromination of paeonol with bromine and copper(Ⅱ)bromide was studied.The target compounds were different because of the different solvents.When paeonol was brominated with reagents like bromine in anhydrous diethyl ether and anhydrous aluminium trichloride,5bromo4methoxy2hydroxyacetophenone was obtained.The yield was 445%.Like cupric bromide in chloroformethyl acetate and anhydrous ethanol,the yield we obtained ωbromo4methoxy5bromo2hydroxyacetophenone was 475%.Paeonol was selectively brominated by copper(Ⅱ)bromide in anhydrous methanol(or chloroformethyl acetate)to give ωbromo4methoxy2hydroxyacetophenone in yield of 633%(or 487%).The structures of the target compounds were characterized by IR,1H NMR and MS.
出处 《化学研究与应用》 CAS CSCD 北大核心 2003年第4期577-578,共2页 Chemical Research and Application
基金 科技部重点科技项目([2001]528001EP09001) 重庆市教委自然基金([2001]12)。
关键词 芍药酮 溴化反应 溴化铜 中药 牡丹皮 活性成分 copper(Ⅱ)bromide bromine brominatiom
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