Double metal cyanides as efficient solid acid catalysts for synthesis of beta-amino alcohols under solvent-free conditions

TitleDouble metal cyanides as efficient solid acid catalysts for synthesis of beta-amino alcohols under solvent-free conditions
Publication TypeJournal Article
Year of Publication2008
AuthorsSaikia, L, Satyarthi, JK, Gonnade, RG, Srinivas, D, Ratnasamy, P
JournalCatalysis Letters
Volume123
Issue1-2
Pagination24-31
Date PublishedJUN
Type of ArticleArticle
ISSN1011-372X
Keywordsbeta-Amino alcohols, double metal cyanide (DMC), regioselective ring-opening of epoxides, Single crystal x-ray structure, solid Lewis-acid catalyst
Abstract

A novel application of Fe-Zn double metal cyanide complexes as solid, acid catalysts for regioselective synthesis of beta-amino alcohols under solvent-free conditions via ring-opening of epoxides with amines is reported for the first time. The conversion of epoxides to beta-amino alcohols is nearly 100%. In the reaction with styrene oxide, regioselective beta-amino alcohol formation is higher with aromatic than with aliphatic amines. Strong Lewis acidic Zn(2+) ions in the catalyst are probably the active sites in this reaction.

DOI10.1007/s10562-008-9410-z
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)2.294
Divison category: 
Catalysis and Inorganic Chemistry
Center for Material Characterization (CMC)
Physical and Materials Chemistry