IMPROVED SYNTHESIS OF QUINALDINES BY THE SKRAUP REACTION

被引:15
作者
SONG, ZG
MERTZMAN, M
HUGHES, DL
机构
[1] Department of Process Research, Merck & Co, Inc., Rahway, New Jersey
关键词
D O I
10.1002/jhet.5570300103
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of substituted quinaldines was synthesized with much improved yields from the reaction of crotonaldehyde and the corresponding anilines using either p-chloranil or 2,3-dichloro-1,4-naphthoquinone as the oxidant.
引用
收藏
页码:17 / 21
页数:5
相关论文
共 5 条
[2]  
JONES G, 1977, CHEM HETEROCYCLIC 1, V32
[3]   IMPROVEMENT IN DOEBNER-MILLER SYNTHESIS OF QUINALDINES [J].
LEIR, CM .
JOURNAL OF ORGANIC CHEMISTRY, 1977, 42 (05) :911-913
[4]   QUINALDINE AND 4-HYDROXYQUINALDINE DERIVATIVES FROM META-CHLOROANILINE AND META-TOLUIDINE [J].
SPIVEY, AM ;
CURD, FHS .
JOURNAL OF THE CHEMICAL SOCIETY, 1949, (OCT) :2656-2662
[5]   Improved syntheses of quinaldines and 3-alkyl quinolines [J].
Utermohlen, WP .
JOURNAL OF ORGANIC CHEMISTRY, 1943, 8 (06) :544-549