The synthetic method of dithianon intermediate 2,3-dichloro-1,4-naphthoquinone was introduced. Starting with raw material sodium 4-amino1-naphthalene sulfonate, 2,3-dichloro-1,4-naphthoquinone was synthesized through ...The synthetic method of dithianon intermediate 2,3-dichloro-1,4-naphthoquinone was introduced. Starting with raw material sodium 4-amino1-naphthalene sulfonate, 2,3-dichloro-1,4-naphthoquinone was synthesized through acidification, chlorination and oxidation. After filtration and recrystallization, more than 98% of 2,3-dichloro-1,4-naphthoquinone was obtained, and the yield reached 76%(measured by sodium 4-amino-1-naphthalene sulfonate).展开更多
In this study, bergapten was synthesized in a yield of 55% from phloroglucinol as starting material, via a novel approach including monomethylation, Hoesch reaction, acetylation, deacetoxylation, Pechmann condensation...In this study, bergapten was synthesized in a yield of 55% from phloroglucinol as starting material, via a novel approach including monomethylation, Hoesch reaction, acetylation, deacetoxylation, Pechmann condensation and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone(DDQ) dehydrogenation. With the adoption of the acetylation of enol tautomer, the deacetoxylation and the DDQ dehydrogenation, the novel approach differs greatly from the processes reported previously, though the starting material was the same or similar to those used on previous synthetic processes. The newly adopted reaction underwent easily, affording all reactions in high yields, especially acetylation and deacetoxylation and DDQ dehydrogenation in almost quantitative yields, ensuring a final yield higher than those previously reported.展开更多
文摘The synthetic method of dithianon intermediate 2,3-dichloro-1,4-naphthoquinone was introduced. Starting with raw material sodium 4-amino1-naphthalene sulfonate, 2,3-dichloro-1,4-naphthoquinone was synthesized through acidification, chlorination and oxidation. After filtration and recrystallization, more than 98% of 2,3-dichloro-1,4-naphthoquinone was obtained, and the yield reached 76%(measured by sodium 4-amino-1-naphthalene sulfonate).
基金supported by the Project of Department of Science and Technology of Zhejiang Province, China (No.2021C04021).
文摘In this study, bergapten was synthesized in a yield of 55% from phloroglucinol as starting material, via a novel approach including monomethylation, Hoesch reaction, acetylation, deacetoxylation, Pechmann condensation and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone(DDQ) dehydrogenation. With the adoption of the acetylation of enol tautomer, the deacetoxylation and the DDQ dehydrogenation, the novel approach differs greatly from the processes reported previously, though the starting material was the same or similar to those used on previous synthetic processes. The newly adopted reaction underwent easily, affording all reactions in high yields, especially acetylation and deacetoxylation and DDQ dehydrogenation in almost quantitative yields, ensuring a final yield higher than those previously reported.
