Effect of substitution degree of 2-hydroxypropyl-β-cyclodextrin on the alkaline hydrolysis of cinnamaldehyde to benzaldehyde
Abstract
The yield of benzaldehyde in the 2-hydroxypropyl-β-cyclodextrin (2-HP-β-CD), with a low degree of substitution (DS = 3.9), catalytic system was 70%, which was higher than that of the system with 8.8 DS under the optimised conditions (323 K, 2% NaOH (w/v), cinnamaldehyde:2-HP-β-CD = 1:1 (molar ratio)). Due to the structural complementary effects of the host and guest, cyclodextrins (CDs) played the catalysis role in the reaction, which was...
Paper Details
Title
Effect of substitution degree of 2-hydroxypropyl-β-cyclodextrin on the alkaline hydrolysis of cinnamaldehyde to benzaldehyde
Published Date
Feb 5, 2014
Journal
Volume
26
Issue
10-12
Pages
796 - 803
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