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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1390088Erstellt: 26. Oktober 2026

Sulfuric Acid → 4[2{2(4-Sulfophenyl)ethylsulfonyl}4-nitrophenylazo]5-morpholinosulfonamido-1-naphthol

https://huagongshe.com/reaction/1390088

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktSodium AcetateHCID 517045—
Edukt2[2(4-Sulfophenyl)ethylsulfonyl]-4-nitroanilineHCID 20294866—
Edukt5-Morpholinosulfonamido-1-naphtholHCID 20294875—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt4[2{2(4-Sulfophenyl)ethylsulfonyl}4-nitrophenylazo]5-morpholinosulfonamido-1-naphtholHCID 136109379—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To 3 ml. of conc. sulfuric acid under cooling was added 0.43 g. of sodium nitrite, dissolved by heating and, after cooling, 5.5 ml. of acetic acid were added thereto. The resulting solution was cooled to 5° C. and 2.32 g. of 2[2(4-sulfophenyl)ethylsulfonyl]-4-nitroaniline were added thereto with stirring. Stirring was continued at room temperature for 3 hours to prepare a diazonium salt solution. Separately, a solution of 1.85 g. of 5-morpholinosulfonamido-1-naphthol in 250 ml. of ethanol and 30 ml. of water was prepared, and a solution of 15 g. of sodium acetate in 40 ml. of water was added thereto with stirring. To the resulting solution, the diazonium salt solution as prepared above was added dropwise under ice-cooling. The reaction mixture was stirred at about 50° C. for 2 hours. Thereafter, the mixture was concentrated to about 100 ml., the precipitate thus separated was recovered by filtration and dried to give 4.3 g. of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04247629
Quelldatensatzuspto-grants-1981_01
ORD IDord-4b9cac2f78474071ac80be99cc349107
Quellennotizuspto-grants-1981_01