Papers by Keyword: Acylation Reaction

Abstract: A series of epicatechin derivatives, including 3-O-palmitoyl epicatechin, 3-O-myristoyl epicatechin, 3-O-lauroyl epicatechin, 3-O-decanoyl epicatechin and 3-O-octanoyl epicatechin, were prepared by the acylation method. Structures of these prepared products were characterized by LC/MS and ¹H-NMR spectroscopy. Their antioxidant activity were assessed by the methods of DPPH and ABTS free radical scavenging. The results showed that aliphatic acyl epicatechin derivatives with varying aliphatic groups were synthesized by this method. The antioxidant activity of aliphatic acyl epicatechin derivatives were better than the oil-soluble tea polyphenol and BHT, equal to TBHQ.

Abstract: 1,2-aceanthrylenedione was synthesized through the acylation reaction of anthracene and oxalyl chloride catalyzed by anhydrous AlCl3. The effects of various reaction conditions on the yield and selectivity of 1, 2-aceanthrylenedione were studied by GC analysis. The results show that the optimum synthesis conditions of the acylation reaction are as follows : the molar ratio of oxalyl chloride to anthracene being 1:2, the molar ratio of anhydrous AlCl3 to anthracene being 4:1, the reaction time being 5 h, the reaction temperature being 303k and the solvent of the reaction system being CS2. Under those conditions, the yield and selectivity of 1, 2-aceanthrylenedione is 83.8 % and 92.3% respectively. Pure 1, 2-aceanthrylenedione was prepared by extraction and recrystallation. The structure of 1, 2-aceanthrylenedione was identified by measure of melting point, GC/MS, FTIR and 1HNMR analyses.