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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >A CONVENIENT SYNTHESIS OF NEW 1-ALKYNYL-1H-BENZOTRIAZOLES BY REACTION OF ALKYNYL(PHENYL)IODONIUM SALTS WITH BENZOTRIAZOLE ION
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A CONVENIENT SYNTHESIS OF NEW 1-ALKYNYL-1H-BENZOTRIAZOLES BY REACTION OF ALKYNYL(PHENYL)IODONIUM SALTS WITH BENZOTRIAZOLE ION

机译:炔基(苯基)碘鎓盐与苯并三唑离子的反应方便地合成新型1-炔基-1H-苯并三唑

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摘要

The reaction of arylethynyl(phenyl)iodonium tosylates with benzotriazole ion gave new 1-alkynyl-1H-benzotriazoles in good yields. This result indicates that alkynyliodonium salts can be used for direct alkynylation of benzotriazole. However,the similar reactions of (tertbutylethynyl)(phenyl)iodonium and 1-octynyl (phenyl)iodonium tosylates do not afford the 1-alkynyl-1H-benzotriazoles but alkenylbenzotriazoles via the reaction of alkylidenecarbenes.
机译:芳基乙炔基(苯基)碘化甲苯磺酸盐与苯并三唑离子的反应以良好的收率得到了新的1-炔基-1H-苯并三唑。该结果表明炔炔碘鎓盐可用于苯并三唑的直接炔基化。然而,(叔丁基乙炔基)(苯基)碘鎓和1-辛炔基(苯基)碘代甲苯磺酸酯的相似反应不能通过亚烷基卡宾的反应得到1-炔基-1H-苯并三唑而是烯基苯并三唑。

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