Reactions of 1-(. alpha.-alkoxyalkyl)-and 1-(. alpha.-(aryloxy) alkyl) benzotriazoles with the Grignard reagents. A new and versatile method for the preparation of ethers

AR Katritzky, S Rachwal, B Rachwal

文献索引：Katritzky, Alan R.; Rachwal, Stanislaw; Rachwal, Bogumila Journal of Organic Chemistry, 1989 , vol. 54, # 26 p. 6022 - 6029

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被引用次数: 68

摘要

1-(a-Alkoxyalky1) benzotriazoles deriving from aldehydes (other than formaldehyde), or from ketones, react with Grignard reagents at 110 “C to provide a high-yielding, general synthesis of dialkyl and alkyl aryl ethers. Under similar conditions, 1-(alkoxymethy1)-and 1-((ary1oxy) methyl) benzotriazoles give, by a different cleavage pattern of the NC-0 grouping, 1- alkylbenzotriazoles and N, N'-dialkyl-o-phenylenediamines. The 1-(a-alkoxyalky1) ...