摘要
以对氯苄基叠氮和乙酰丙酮为原料合成5-甲基-4-乙酰基-1-对氯苄基-1,2,3-三唑,考察了催化剂类型、溶剂、配比对反应的影响,并确定了优化的工艺条件:无水碳酸钾为催化剂,乙腈和乙醇等体积混合为反应溶剂,n(对氯苄基叠氮)∶n(乙酰丙酮)=1∶1.2,反应时间2 h。产品收率达94%,目标化合物的结构经1H NMR和IR确证。
1-(4-Chlorobenzyl)-4-acetyl-5-methyl-1,2,3-triazole was synthesized from 1-(azidomethyl)-4-chlorobenzene and acetylacetone.Best results with 94% yield were obtained under conditions of catalyst of anhydrous potassium carbonate,reaction dissolvent of acetonitrile and ethanol(1∶1),molar ratio of 1-(azidomethyl)-4-chlorobenzene to acetylacetone of 1 to 1.2 and reaction time of 2 h.The structure of the title compound was confirmed by 1H NMR and IR.
出处
《精细化工中间体》
CAS
2012年第4期42-44,共3页
Fine Chemical Intermediates
基金
国家自然科学基金青年科学基金(21102003)
安徽理工大学人才引进启动基金
安徽理工大学青年教师科学研究基金
关键词
对氯苄基叠氮
1
2
3-三唑
合成
1-(azidomethyl)-4-chlorobenzene
1,2,3-triazole
synthesis