Reaction of 2-aminobenzimidazole with acetylene
Publication type: Journal Article
Publication date: 1992-03-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 15739171
General Chemistry
General Computer Science
Abstract
The reaction of 2-aminobenzimidazole (1) with acetylene under pressure proceeds with the formation of vinyl monomers, corresponding to amine and imine forms, 1-vinyl-2-amino- and 1,3-divinyl-2-iminobenzimidazoles, depending on the reaction conditions. 1,3-Divinyl-2-benzimidazolone was also isolated in aqueous dioxane in addition to the monovinyl derivative of1. Cyclization of the divinyl derivative of1 with acetylene proceeds to give 9-vinyl-1,2-dimethylimidazo[1,2-a]-benzimidazole.
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Baikalova L. V., Domnina E. S., Afonin A. V. Reaction of 2-aminobenzimidazole with acetylene // Russian Chemical Bulletin. 1992. Vol. 41. No. 3. pp. 588-589.
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Baikalova L. V., Domnina E. S., Afonin A. V. Reaction of 2-aminobenzimidazole with acetylene // Russian Chemical Bulletin. 1992. Vol. 41. No. 3. pp. 588-589.
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RIS
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TY - JOUR
DO - 10.1007/bf00863093
UR - https://doi.org/10.1007/bf00863093
TI - Reaction of 2-aminobenzimidazole with acetylene
T2 - Russian Chemical Bulletin
AU - Baikalova, L V
AU - Domnina, E S
AU - Afonin, A V
PY - 1992
DA - 1992/03/01
PB - Springer Nature
SP - 588-589
IS - 3
VL - 41
SN - 1066-5285
SN - 1573-9171
ER -
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BibTex (up to 50 authors)
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@article{1992_Baikalova,
author = {L V Baikalova and E S Domnina and A V Afonin},
title = {Reaction of 2-aminobenzimidazole with acetylene},
journal = {Russian Chemical Bulletin},
year = {1992},
volume = {41},
publisher = {Springer Nature},
month = {mar},
url = {https://doi.org/10.1007/bf00863093},
number = {3},
pages = {588--589},
doi = {10.1007/bf00863093}
}
Cite this
MLA
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Baikalova, L. V., et al. “Reaction of 2-aminobenzimidazole with acetylene.” Russian Chemical Bulletin, vol. 41, no. 3, Mar. 1992, pp. 588-589. https://doi.org/10.1007/bf00863093.