Phenyl cyclopropyl ether in electrophilic substitution reactions
作者:
A.A.Petinskii,
S.M.Shostakovskii,
É.I.Kositsyna,
期刊:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science
(Springer Available online 2004)
卷期:
Volume 21,
issue 8
页码: 1720-1723
ISSN:0568-5230
年代: 2004
DOI:10.1007/BF00851187
出版商: Springer_US-Boston
数据来源: Springer
摘要:
1.The three-membered ring of cyclopropyl phenyl ether is stable in halogenation and acylation reactions, while the cyclopropoxy group exhibits a para-orienting effect.2.The nitration of cyclopropyl phenyl ether with dilute HNO3solution is accompanied by a cleavage of the three-membered ring, with the formation of 2,4-dinitrophenol and propionaldehyde.
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