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Synthesis of π‐Extended Carbazoles via One‐Pot C—C Coupling and Chlorination Promoted by FeCl 3
Author(s) -
Qian Yang,
Shang Jia,
Lyu ZhenHua,
Huang Xin,
Guan Aijiao,
Xu LiJin,
Gong HanYuan
Publication year - 2020
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.202000230
Subject(s) - chemistry , carbazole , yield (engineering) , catalysis , surface modification , one pot synthesis , combinatorial chemistry , medicinal chemistry , carbon fibers , stereochemistry , organic chemistry , materials science , composite number , metallurgy , composite material
Summary of main observation and conclusion A facile synthesis, functionalization, and emission property of N‐doped carbon‐rich halogenated compound 3,6,12,15‐tetrachloro‐9‐phenyl‐9H‐tetrabenzo[a,c,g,i]carbazole ( ClCbz ) was reported. Cost‐effective FeCl 3 catalyst serves to break eight C—H bonds of 1,2,3,4,5‐pentaphenylpyrrole ( 1 ) and subsequently construct two C—C and four C—Cl bonds in one pot with a high yield of up to 75%.
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