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合成了一种新的1,5-二酮类化合物,并通过高效液相色谱(HPLC)、差示扫描量热(DSC)、核磁共振氢谱(1HNMR)、核磁共振碳谱(13CNMR)、质谱(MS)等分析方法对其化学结构进行了表征,推断出该物质为1,3,5-三[4-(二甲基氨基)苯]-1,5-二戊酮。
Abstract:A new kind of 1,5-diketones compound was synthesized in the experiments. The structuralwas characterized by HPLC,DSC,1HNMR,13 CNMR and MS. This compound was inferenced as 1,3,5-tris[4-(dimethylamino)phenyl]-1,5-Pentanedione.
[1]KEVIN T P,MICHAEL C,PHILIP R,et al,Ketene dithio acetals as synthetic intermediates.synthesis of unsaturated 1,5-diketones[J].Journal of American Chemical Society,1981,103(12):3584-3585.
[2]STEPHEN S H,WILLIAM J B,Base-catalyzed alkylation of cyclopentadiene rings with alcohols and amines[J].Journal of Organic Chemical,1978,43(21):4090-4094.
[3]YEHIA N A M,POLBORN K,MULLER T J J:A novel four component one-pot access to pyrindines and tetrahydroquinolines[J].Tetrahedron Letters,2002,43(39):6907-6910.
[4]REEMA K T,WILLIAM R R.Remarkable phosphine-effect on the intramolecular aldol reactions of unsaturated 1,5-Diketones:highly regioselective synthesis of cross-conjugated dienones[J].Journal of American Chemical Society,2005,127(48):16778-16779.
[5]刘万毅,李金夫,马永祥,等.1,5-二芳基二酮衍生物的制备—无水溶剂状态下苯乙酮与芳基烯酮的共轭加成反应研究[J].高等学校化学学报,2001,22(10):141-144.
[6]王克虎,殷雪娇,陶瑞,等,无溶剂研磨法快速合成3-芳乙烯基-1,5-二酮类化合物的反应研究[J].有机化学,2016,36(1):113-120.
[7]DAVID C H,JOANNE C H.A short synthesis ofα-herbertenol featuring the use of a dihydropyranone as a 1,5-diketone synthon[J].Tetrahedron Letters,1998,39(51):9573-9574.
[8]DAVID C H,JOANNE C H.1,5-Diketones from 3,4-dihydropyranones:an application in the synthesis of(±)-α-herbertenol[J].Tetrahedron,1999,55(30):9333-9340.
基本信息:
DOI:10.16389/j.cnki.cn42-1737/n.2017.03.004
中图分类号:O625.42
引用信息:
[1]胡丽,刘小成,邓嘉伦,等.一种新的1,5-二酮类化合物的结构表征[J].江汉大学学报(自然科学版),2017,45(03):214-218.DOI:10.16389/j.cnki.cn42-1737/n.2017.03.004.