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Synthesis of 2‐Phenylquinoline and its Derivatives by Multicomponent Reaction of Aniline, Benzylamine, Alcohols, and CCl4 Catalyzed by FeCl3·6H2O
Journal of Heterocyclic Chemistry ( IF 2.0 ) Pub Date : 2015-01-23 , DOI: 10.1002/jhet.2394 Ravil Khusnutdinov 1 , Alfiya Bayguzina 1 , Rishat Aminov 1 , Usein Dzhemilev 1
Journal of Heterocyclic Chemistry ( IF 2.0 ) Pub Date : 2015-01-23 , DOI: 10.1002/jhet.2394 Ravil Khusnutdinov 1 , Alfiya Bayguzina 1 , Rishat Aminov 1 , Usein Dzhemilev 1
Affiliation
2‐Phenylquinolines, 2‐phenyl‐3‐methyl‐quinolines, and 2‐phenyl‐3‐ethylquinolines were synthesized in high yields (78–90%) by the reaction of aniline, benzylamine, aliphatic alcohols (ethanol, n‐propanol, n‐butanol), and CCl4 catalyzed by FeCl3·6H2O in tetrachloromethane.
中文翻译:
FeCl3·6H2O催化苯胺,苄胺,醇和CCl4的多组分反应合成2-苯基喹啉及其衍生物
通过苯胺,苄胺,脂族醇(乙醇,正丙醇,苯胺)的反应,可以高产率(78-90%)合成2-苯基喹啉,2-苯基-3-甲基喹啉和2-苯基-3-乙基喹啉。正丁醇)和FeCl 3 ·6H 2 O在四氯甲烷中催化的CCl 4。
更新日期:2015-01-23
中文翻译:
FeCl3·6H2O催化苯胺,苄胺,醇和CCl4的多组分反应合成2-苯基喹啉及其衍生物
通过苯胺,苄胺,脂族醇(乙醇,正丙醇,苯胺)的反应,可以高产率(78-90%)合成2-苯基喹啉,2-苯基-3-甲基喹啉和2-苯基-3-乙基喹啉。正丁醇)和FeCl 3 ·6H 2 O在四氯甲烷中催化的CCl 4。