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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 79351Erstellt: 23. Oktober 2026

Iodine → HCID 178526562, Verbindung

https://huagongshe.com/de/reaction/79351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktPotassium HydroxideHCID 14797—
Edukt4-NitroindazoleHCID 18057—
EduktSodium BisulfiteHCID 23665763—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178526562HCID 17852656284,8%

Reaktionsschritte

A solution of 4-nitro-1H-indazole (50.0 g; 306 mmol) in N,N-dimethylformamide (600 mL) was cooled to 5° C. under a nitrogen atmosphere with stirring. Powdered potassium hydroxide (68.8 g; 1226 mmol) was added. A solution of iodine (156 g; 613 mmol) in DMF (200 mL) was added slowly to the reaction mixture over 2 hours maintaining the temperature between 5 and 10° C. The mixture was stirred at 25° C. for 24 hours. Additional iodine (39.0 g; 153.2 mmol) and potassium hydroxide (17.2 g; 306.5 mmol) was added. The mixture was stirred at 25° C. for a further 12 hours. The reaction mixture was added to an aqueous solution of sodium bisulfite (10% solution; 3300 mL) with stirring. The resulting precipitate was collected by filtration and washed with water. The material was dried in a vacuum oven at 40° C. The material was dissolved in methylene chloride/methanol (10:1; 1.5 L) and filtered through Celite® to remove inorganic impurities. Concentration of the solution under vacuum gave 3-iodo-4-nitro-1H-indazole as a yellow solid (75 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841455B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8fd7602e27f64a30b95606b1836bde8a
Quellennotizuspto-grants-2014_09