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新型去氢枞基1,3,4-噁二唑的合成与表征     被引量:7

Synthesis and characterization of novel dehydroabietyl-1,3,4-oxadiazoles

文献类型:期刊文献

中文题名:新型去氢枞基1,3,4-噁二唑的合成与表征

英文题名:Synthesis and characterization of novel dehydroabietyl-1,3,4-oxadiazoles

作者:韩春蕊[1] 宋湛谦[1] 商士斌[1] 高宏[1]

第一作者:韩春蕊

机构:[1]中国林业科学研究院林产化学工业研究所

年份:2007

卷号:27

期号:8

起止页码:42-44

中文期刊名:现代化工

外文期刊名:Modern Chemical Industry

收录:CSTPCD;;Scopus;北大核心:【北大核心2004】;CSCD:【CSCD2011_2012】;

语种:中文

中文关键词:去氢枞基;酰肼;噁二唑;芳基;合成

外文关键词:dehydroabietyl; hydrazine; oxadiazole; aryl; synthesis

分类号:TQ225.24

摘要:以去氢枞酸为原料,经酰化得到酰氯,酰氯与85%(质量分数)水合肼反应制备出去氢枞酰肼,去氢枞酰肼再与5种芳香酰氯反应得N,N′-二酰基肼,其再经POCl3脱水闭环反应,合成了5种新的2-去氢枞基-5-芳基-1,3,4-二唑。研究了合成反应条件;每步收率均在75%以上。
Five novel 2-dehydroabietyl-5-aryl-1, 3, 4-oxadiazoles were synthesized by cyclization of N, N'- diacylhydrazines with POCl3. N, N'-diacylhydrazines were obtained via reacting dehydroabietyl hydrazine, which is prepared by dehydroabietic acid with PCl3 or SOCl2 and then 85% (mass ratio) NH2NH2·H2O, with aryl chloride. The synthesis conditions were studied, and the yield of every step is more than 75 %.

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