首页> 外文期刊>The Journal of Organic Chemistry >Esters as Acylating Reagent in a Friedel-Crafts Reaction: Indium Tribromide Catalyzed Acylation of Arenes Using Dimethylchlorosilane
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Esters as Acylating Reagent in a Friedel-Crafts Reaction: Indium Tribromide Catalyzed Acylation of Arenes Using Dimethylchlorosilane

机译:酯在弗瑞德-克拉夫茨反应中的酰化试剂:使用二甲基氯硅烷的三溴化铟催化芳烃酰化

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摘要

The Friedel-Crafts acylation of arenes with esters by dimethylchlorosilane and 10 mol % of indium tribromide has been achieved. The key intermediate RCOOSi(Cl)Me-2 is generated from alkoxy esters with the evolution of the corresponding aikanes. The scope of the alkoxy ester moiety was wide: tert-butyl, benzyl, allyl, and isopropyl esters were successful. In addition. we demonstrated the direct synthesis of the indanone intermediate 11 of salviasperanol from ester 10.
机译:通过二甲基氯硅烷和10mol%的三溴化铟实现了芳烃与酯的弗瑞德-克来福特酰化。关键中间体RCOOSi(Cl)Me-2是由烷氧基酯生成的,并伴随有相应的烷烃的生成。烷氧基酯部分的范围很广:叔丁基,苄基,烯丙基和异丙基酯是成功的。此外。我们证明了由酯10直接合成丹参戊醇的茚满酮中间体11。

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