Bibliographic Citation
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Title | Kinetics of the aminolysis of 1-phenoxy-2,3-propylene carbonate with benzylamine in chlorobenzene |
Creator/Author | Stroganov, V.F. ; Savchenko, V.N. ; Titskii, G.D. ; Sidorenko, E.V. ; Zaitsev, u.S. |
Publication Date | 1988 Aug 10 |
OSTI Identifier | OSTI ID: 6008398 |
Other Number(s) | CODEN: JOCYA |
Resource Type | Journal Article |
Resource Relation | J. Org. Chem. USSR (Engl. Transl.) ; Vol/Issue: 24:3; Translated from Zh. Org. Khim.; 24: No. 3, 500-503 (Mar 1988) |
Research Org | Ukrainian Scientific-Research Institute of Plastics, Donetsk (USSR) |
Subject | 400201 -- Chemical & Physicochemical Properties; AMINES-- CATALYTIC EFFECTS;CARBONIC ACID ESTERS-- CATALYSIS;CHLORINATED AROMATIC HYDROCARBONS-- SOLVENT PROPERTIES; ACTIVATION ENERGY;CATALYSTS;CHEMICAL BONDS;CHEMICAL REACTION KINETICS;HYDROGEN;INFRARED SPECTRA;LYSIS;QUANTITY RATIO;SPECTROPHOTOMETRY |
Related Subject | AROMATICS;ELEMENTS;ENERGY;ESTERS;HALOGENATED AROMATIC HYDROCARBONS;KINETICS;NONMETALS;ORGANIC CHLORINE COMPOUNDS;ORGANIC COMPOUNDS;ORGANIC HALOGEN COMPOUNDS;REACTION KINETICS;SPECTRA |
Description/Abstract | The kinetics of the reaction of 1-phenoxy-2,3-propylene carbonate with benzylamine in chlorobenzene at 60/degree/C were studied.^Aminolysis of the cyclic carbonate takes place in two parallel directions, i.e., noncatalytic and catalyzed by two molecules of benzylamine.^A mechanism is proposed for the catalytic reaction, involving reaction of the cyclic carbonate, activated by a hydrogen bond with the amine, and the self-associated amine through a six-membered cyclic transition state. |
Country of Publication | United States |
Language | English |
Format | Pages: 445-448 |
System Entry Date | 2001 May 13 |
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