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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 Date1988 Aug 10
OSTI IdentifierOSTI ID: 6008398
Other Number(s)CODEN: JOCYA
Resource TypeJournal Article
Resource RelationJ. Org. Chem. USSR (Engl. Transl.) ; Vol/Issue: 24:3; Translated from Zh. Org. Khim.; 24: No. 3, 500-503 (Mar 1988)
Research OrgUkrainian Scientific-Research Institute of Plastics, Donetsk (USSR)
Subject400201 -- 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 SubjectAROMATICS;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 PublicationUnited States
LanguageEnglish
FormatPages: 445-448
System Entry Date2001 May 13

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