化学学报 ›› 1955, Vol. 21 ›› Issue (3): 268-272. 上一篇    下一篇

论文

芳香基氟硼酸重氮盐于氯化乙基汞及二乙基汞的反应

胡秉方   

  1. 北京农业大学
  • 投稿日期:1955-05-17 发布日期:2013-06-04

THE REACTION OF ARYLDIAZONIUM FLUOROBORATE WITH ETHYL MERCURIC CHLORIDE AND DIETHYL MERCURY

HU PING-FANG(PIN-FONG HU)   

  • Received:1955-05-17 Published:2013-06-04

Hodgson等曾企圖利用重氮鹽的氯化鋅的複鹽與Grignard試劑反應,希望能將烴基引入芳香環;伹在反應產物中,並無所預期的芳香烴,而有不同此例的Ar·Ar,Ar·H,ArN=N·Ar,Ar·N=N·R及Ar·X.根據最近等對芳香基氟硼酸重氮鹽的研究,證明芳香基氟硼酸重氮鹽在分解時產生烴離子,而與其它重氮鹽產生烴自由基者不同.作者因此利用芳香基氟硼酸重氮鹽及較Grignard試劑的活潑性小的有機汞化合物來代替芳香基重氮鹽的氯化鋅複鹽及Grignard試劑.在反應產物中,並無乙基芳香烴存在;生成的是不同量的Ar·Ar,Ar·H,Ar·Cl等,結果與Hodgson的實驗基本上相同.

An attempt was made by Hodgson to introduce alkyl or aryl group into aromatic ring through the reaction between aryldiazonium chloride [(ArN2 Cl)2·ZnCl2] and Grignard reagent(RMgX).Among the reaction products, however, he found Ar·Ar, Ar·H, ArN=NAr, ArN=N·R, Ar·X present in various proportions, but no Ar·R as expected.According to the result of an recent investigation of A.N.Nesmeyanov, the thermal decomposition of aryldiazonium fluoroborate afforded aryl ration, while the diazonium salt of other types gave aryl radical under the same conditions.