Tungstosilicic acid (H4SiW12O40) have efficient catalysts for synthesis of 2,3-Dihydroxynaphthoquinone from lawsone
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Date
2016
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Abstract
The Thiele–Winter reaction is of interest for synthesis of tetracetoxyaromatic precursors of hydroxynaphtoquinones. Solid acids such as
Tungstosilicic acid (H4
SiW12O40) have an efficient catalyst in acetoxylation reaction of naphtoquinones without the use of organic solvent
at room temperature. 1,2,3,4-Tetrahydroxynaphthalene was easily oxidized at room temperature in 2,3-Dihydroxynaphthoquinone
by using (Pc[Co]/K10) and air (1 atm). We have also tested this type of reaction in 2-hydroxynaphthoquinone (Lawsone). Many
naphthoquinones are natural products with interesting biological properties
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Keywords
Heteropolyacids, Without solvent, Room temperature, Lawsone, Catalytic system (Pc[Co]/K10)
