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HRID 1656859作成日:2026年10月26日

Sulfite → 1,4,5,8-Naphthalenetetracarboxylic acid

https://huagongshe.com/reaction/1656859

反応式

関与物質

役割名称HCID仕込み量
反応物SulfiteHCID 1099—
反応物1,4,5,8-Naphthalenetetracarboxylic acidHCID 31422—
反応物[2-adenin-9-yl-5-[[[[5-(3-carbamoyl-4H-pyridin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-oxido-phosphoryl]oxy-oxido-phosphoryl]oxymethyl]-4-hydroxy-tetrahydrofuran-3-yl] phosphateHCID 12598259—
生成物1,4,5,8-Naphthalenetetracarboxylic acidHCID 31422—
生成物DisodiumHCID 141233—

反応手順

The process as claimed in claim 9, wherein, after the oxidation has ended, the reaction mixture is subjected to a heat treatment at a temperature of between 90° and 100° C. under the autogenous pressure of 1 to 5 bar which is established, in the presence of sulfite, the resulting suspension of the tetrasodium salt of naphthalene-1,4,5,8-tetracarboxylic acid is cooled, after the reaction vessel has been let down, to a temperature of 20° to 30° C. the pH is then adjusted to 4.5 to 5 by acidification, the resulting disodium salt of naphthalene-1,4,5,8-tetracarboxylic acid is isolated, this salt is converted into the tetrasodium salt of naphthalene-1,4,5,8-tetracarboxylic acid in an aqueous alkali metal hydroxide solution and, optionally after removal of insoluble impurities, naphthalene-1,4,5,8-tetracarboxylic acid 1,8-monoanhydride is precipitated by acidification to a pH of less than 1 at a temperature of 80° to 100° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05254796
出典データセットuspto-grants-1993_10
ORD IDord-6b19443ace4141118d6eedec8f96c519
出典メモuspto-grants-1993_10