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HRID 4419Erstellt: 23. Oktober 2026

Hydroxide → 2-Hydroxy-5-((3,5-bis(methoxycarbonyl)phenyl)azo)benzeneacetic acid

https://huagongshe.com/de/reaction/4419

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroxideHCID 961—
Edukt(2-Hydroxyphenyl)acetic acidHCID 11970—
EduktDimethyl 5-aminoisophthalateHCID 66831—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
LösungsmittelSodium HydroxideHCID 14798—
Produkt2-Hydroxy-5-((3,5-bis(methoxycarbonyl)phenyl)azo)benzeneacetic acidHCID 127324—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

20.9 g of dimethyl-5-amino-benzene-1,3-dicarboxylate was dissolved in 20 ml of concentrated hydrochloric acid in 200 ml of ice water. The solution was diazotized with 7 g of sodium nitrite dissolved in 30 ml of water. 30.4 g of 2-hydroxy-phenylacetic acid was dissolved in 200 ml of water and 24 g of sodium hydroxide. The solution was cooled with 100 g of ice. To this hydroxide solution was then added the diazonium salt solution, all at once, and with vigorous stirring. After 30 seconds the solution was acidified with acetic acid and the precipitate was filtered off. The precipitate was leached with an about 25% ethanol solution which was then diluted with water until a state of weak opalescence was reached. The solution was treated with active carbon and evaporated down to half its volume. Sodium hydrogen carbonate was added until the solution was clear, whereupon the solution was heated (80° C.) and acidified with hydrochloric acid. The solution was cooled, the crystals were filtered off and dried.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04725676
Quelldatensatzuspto-grants-1988_02
ORD IDord-8f9ba23024a24c68b03865b18a945605
Quellennotizuspto-grants-1988_02