首页> 外文期刊>Tetrahedron >Preparation, crystal structure, and spectroscopic, chemical, and electrochemical properties of (2E,4E)-4-[4-(dimethylamino)phenyl]-1-(3-guaiazulenyl)-1,3-butadiene compared with those of (E)-2-[4-(dimethylamino)phenyl]-1-(3-guaiazulenyl)ethylene
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Preparation, crystal structure, and spectroscopic, chemical, and electrochemical properties of (2E,4E)-4-[4-(dimethylamino)phenyl]-1-(3-guaiazulenyl)-1,3-butadiene compared with those of (E)-2-[4-(dimethylamino)phenyl]-1-(3-guaiazulenyl)ethylene

机译:与(E)相比,(2E,4E)-4- [4-(4-(二甲基氨基)苯基] -1-(3-愈创木烯基)-1,3-丁二烯的制备,晶体结构以及光谱,化学和电化学性质)-2- [4-(二甲基氨基)苯基] -1-(3-愈创木烯基)乙烯

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摘要

Wittig reaction of 3-[4-(dimethylamino)phenyl]propanal (5) with (3-guaiazulenylmethyl)triphenylphosphonium bromide (4) in ethanol containing NaOEt at 25 degrees C for 24 h under argon gives the title (2E,4E)-1,3-butadiene derivative 6E in 19% isolated yield. Spectroscopic properties, crystal structure, and electrochemical behavior of the obtained new extended pi-electron system 6E, compared with those of the previously reported (E)-2-[4-(dimethylamino)phenyl]-1-(3-guaiazulenyl)ethylene (12), are documented. Furthermore, reaction of 6E with 1,1,2,2-tetracyanoethylene (TCNE) in benzene at 25 degrees C for 24 h under argon affords a new Diels-Alder adduct 8 in 59% isolated yield. Along with spectroscopic properties of the [pi 4+pi 2] cycloaddition product 8, the crystal structure, possessing a cis-3,6-substituted 1,1,2,2-tetracyano-4-cyclohexene unit, is shown. Moreover, reaction of 6E with (E)-1,2-dicyanoethylene (DCNE) under the same reaction conditions as the above gives no product; however, this reaction in p-xylene at reflux temperature (138 degrees C) for four days under argon affords a new Diels-Alder adduct 9 in 54% isolated yield. Although reaction of 6E with DCNE in toluene at reflux temperature (110 degrees C) for four days under argon provides 9 very slightly, reaction of 6E with dimethyl acetylenedicarboxylate (DMAD) in toluene at reflux temperature for two days under argon yields a new Diels-Alder adduct 10, in 58% isolated yield, which upon oxidation with MnO2 in CH2Cl2 at 25 degrees C for 1 h gives 11, converting a (CH3)(2)N-4 '' into CH3NH-4 '' group, in 37% isolated yield. The crystal structure of 11 supports the molecular structure 10 possessing a partial structure cis-3,6-substituted 1,2-dimethoxycarbonyl-1,4-cyclohexadiene. The title basic studies on the above are reported in detail.
机译:3- [4-(二甲基氨基)苯基]丙醛(5)与(3-愈创木烯基甲基)三苯基溴化((4)在含NaOEt的乙醇中于25°C在氩气中进行Wittig反应24小时,得到标题(2E,4E)- 1,3-丁二烯衍生物6E的分离产率为19%。与先前报道的(E)-2- [4-(4-(二甲基氨基)苯基] -1-(3-愈创木烯基)乙烯相比,获得的新的扩展π电子体系6E的光谱性质,晶体结构和电化学行为(12),有文件证明。此外,在氩气下,6E与1,1,2,2-四氰基乙烯(TCNE)在苯中在25摄氏度下于氩气下于24℃反应24小时,得到了新的Diels-Alder加合物8,分离产率为59%。连同[pi 4 + pi 2]环加成产物8的光谱性质一起,显示了具有顺式-3,6-取代的1,1,2,2-四氰基-4-环己烯单元的晶体结构。另外,在与上述相同的反应条件下,6E与(E)-1,2-二氰基乙烯(DCNE)的反应没有产物。然而,该反应在对二甲苯中在氩气下于回流温度(138摄氏度)下反应四天,从而以54%的分离产率得到了一种新的Diels-Alder加合物9。尽管在氩气下回流温度(110摄氏度)下6E与DCNE在甲苯中反应4天的反应非常轻微,但是在氩气下回流温度下6E与乙炔基二羧酸二甲酯(DMAD)在甲苯中回流两天反应产生了一种新的Diels- der木加合物10,以58%的分离产率,在37℃下用MnO2在CH2Cl2中的氧化反应1小时,得到11,将(CH3)(2)N-4''转变为CH3NH-4''基团。分离产率%。 11的晶体结构支撑具有部分结构顺式3,6-取代的1,2-二甲氧基羰基-1,4-环己二烯的分子结构10。上面详细介绍了标题的基础研究。

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