Hydrochloric acid as an efficient catalyst for intermolecular condensation of alcohols. A simple and highly efficient synthesis of unsymmetrical ethers from benzylic alcohols and alkanols

Verfasser / Beitragende:
[S. Mochalov, A. Fedotov, E. Trofimova, N. Zefirov]
Ort, Verlag, Jahr:
2015
Enthalten in:
Russian Journal of Organic Chemistry, 51/9(2015-09-01), 1217-1231
Format:
Artikel (online)
ID: 605529132
LEADER caa a22 4500
001 605529132
003 CHVBK
005 20210128100816.0
007 cr unu---uuuuu
008 210128e20150901xx s 000 0 eng
024 7 0 |a 10.1134/S107042801509002X  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1134/S107042801509002X 
245 0 0 |a Hydrochloric acid as an efficient catalyst for intermolecular condensation of alcohols. A simple and highly efficient synthesis of unsymmetrical ethers from benzylic alcohols and alkanols  |h [Elektronische Daten]  |c [S. Mochalov, A. Fedotov, E. Trofimova, N. Zefirov] 
520 3 |a Benzylic alcohols and diarylmethanols with electron-donating substituents in the aromatic ring reacted with aliphatic alcohols in the presence of a catalytic amount of HCl to give the corresponding alkyl arylmethyl ethers. The reactivity of diarylmethanols in the intermolecular dehydration depended on the nature of substituents in the aromatic rings and structure of aliphatic alcohol. 
540 |a Pleiades Publishing, Ltd., 2015 
700 1 |a Mochalov  |D S.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
700 1 |a Fedotov  |D A.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
700 1 |a Trofimova  |D E.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
700 1 |a Zefirov  |D N.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
773 0 |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/9(2015-09-01), 1217-1231  |x 1070-4280  |q 51:9<1217  |1 2015  |2 51  |o 11178 
856 4 0 |u https://doi.org/10.1134/S107042801509002X  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a review-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1134/S107042801509002X  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Mochalov  |D S.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Fedotov  |D A.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Trofimova  |D E.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Zefirov  |D N.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119991, Moscow, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/9(2015-09-01), 1217-1231  |x 1070-4280  |q 51:9<1217  |1 2015  |2 51  |o 11178