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Cui, LJ(Cui Lijun)1;Xiao, SY(Xiao Shangyou)1;Yang, HS(Yang Haoshu)1;Xu, P(Xu Pan)1;Cheng, FS(Cheng Fansheng)1;Li, ZH(Li Zhenghua)1;Liang, RH(Liang Ronghui)1;Xia, ZN(Xia Zhining)
ÎÄÌâ:
Investigation on the Reaction Mechanism for the Synthesis of Benzimidazole Derivatives from Aldehydes and o-Phenylenediamine
ÆÚ¿¯Ãû,Äê·Ý,¾í(ÆÚ),ÆðÖ¹Ò³Âë:
À´Ô´³ö°æÎï:CHINESE JOURNAL OF ORGANIC CHEMISTRY ¾í:31 ÆÚ:5 Ò³:672-676
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clijun2004(½ð±Ò+20, ²©Ñ§EPI+1): ·Ç³£¸Ðл£¡ 2011-11-21 17:02:03
UT  WOS:000291508800010

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FN Thomson Reuters Web of Knowledge
VR 1.0
PT  J
AU  Cui, LJ
Xiao, SY
Yang, HS
Xu, P
Cheng, FS
Li, ZH
Liang, RH
Xia, ZN
AF  Cui Lijun
Xiao Shangyou
Yang Haoshu
Xu Pan
Cheng Fansheng
Li Zhenghua
Liang Ronghui
Xia Zhining
TI  Investigation on the Reaction Mechanism for the Synthesis of Benzimidazole Derivatives from Aldehydes and o-Phenylenediamine
SO  CHINESE JOURNAL OF ORGANIC CHEMISTRY
AB  The synthesis of 2-(4-methyphenyl)benzimidazole from 4-methyl benzylaldehyde and o-phenylenediamine was performed. The reaction process was monitored by HPLC, and the structures of related intermediates and products were identified by (1)H NMR, FT-IR and LC-MS techniques. The experiments proved that mono-Schiff base and bis-Schiff base could both be synthesized at the same time when o-phenylenediamine and aldehydes were in a molar ratio of 1 : 1, and the influences of the reaction were proposed.
SN  0253-2786
PD  MAY
PY  2011
VL  31
IS  5
BP  672
EP  676
UT  WOS:000291508800010
ER
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