中國醫藥大學機構典藏 China Medical University Repository, Taiwan:Item 310903500/7518
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    Please use this identifier to cite or link to this item: http://ir.cmu.edu.tw/ir/handle/310903500/7518


    Title: An Efficient and Convenient Method for Synthesis of 1-Substituted Imidazole
    Authors: (Lin, C. M.;);翁豐富(Wong, Fung Fuh)*;(Yeh, M.-Y.)
    Contributors: 藥學院藥物化學研究所
    Keywords: a-Bromo Ketone;1-Substituted Imidazole;1,3-Disubstituted Imidazolium Salt;Lithium Imidazolide
    Date: 2006-07
    Issue Date: 2009-08-26 16:27:51 (UTC+8)
    Abstract: A convenient method for the synthesis 1-substituted imidazoles was developed by the reaction of α-bromoketone with lithium imidazolide. The reaction gave the desired products in improved yields without the formation of 1,3-disubstituted imidazolium salts. Treatment of bromoacetaldehyde ethylene acetal, 2-(bromomethyl)tetrahydro-2H-pyran, and N-(bromomethyl)phthalimide with lithium imidazolide also gave the corresponding 1-substituted imidazole in good to excellent yields. Direct reaction of α-bromoketone with imidazole as control experiment afforded undesired 1,3-disubstituted imidazolium salts with the desired mono-substituted products.
    Relation: HETEROCYCLES 68(7 )1359 ~1370
    Appears in Collections:[Graduate Institute of Pharmaceutical Chemistry] Journal articles

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