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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383003Erstellt: 25. Oktober 2026

Sulfuric Acid → N-acetyl-3-acetoxymethyl-5-(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodoaniline

https://huagongshe.com/reaction/383003

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktDichloromethaneHCID 6344—
EduktAcetic AnhydrideHCID 7918—
Edukt3-Hydroxymethyl-5-(2,3-dihydroxypropylaminocarbonyl)-2,4,6-triiodoanilineHCID 18429181—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
ProduktN-acetyl-3-acetoxymethyl-5-(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodoanilineHCID 18429152—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

3-Hydroxymethyl-5-(2,3-dihydroxypropylaminocarbonyl)-2,4,6-triiodoaniline (3.3 g, 5.3 mmol) was suspended in glacial acetic acid (12 ml) containing acetic anhydride (48 ml) and concentrated sulfuric acid (0.08 ml). The mixture was stirred at 60° C. for 3 h, allowed to cool to room temperature, and CH2Cl2 (100 ml) and water (100 ml) were added. The organic phase was washed with water (3×50 ml) and a saturated aqueous solution of NaHCO3 (2×50 ml). After drying (MgSO4) and evaporation, the residue was dissolved in a mixture of CH2Cl2 and methanol (9:1) and filtered through a short silica pad and evaporated. Yield: 3.0 g (71%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06310243B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-29e9978dcaf94e81b0048e5288bbdc14
Quellennotizuspto-grants-2001_10