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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275779Erstellt: 24. Oktober 2026

1H-Indazol-5-ol → 5-hydroxy-4-(N-phenyliminomethyl)-1H-indazole

https://huagongshe.com/de/reaction/275779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-Indazol-5-olHCID 101438—
EduktMethanimidic acid, N-phenyl-, ethyl esterHCID 111236—
LösungsmittelEthanolHCID 702—
Produkt5-hydroxy-4-(N-phenyliminomethyl)-1H-indazoleHCID 13558159763,5%

Reaktionsbedingungen

Temperatur175 °C

Reaktionsschritte

A round bottomed flask containing a mixture of 5-hydroxy-1H-indazole (28.5 g) and ethyl N—phenylformimidate (35 g) was submerged rapidly in an oil bath pre-heated to 175° C. and the mixture stirred at 160-180° C. for 30 minutes, the ethanol produced in the reaction being removed by distillation. The cooled mixture was then treated with boiling methanol (500 ml) and the resultant brown solid collected by filtration, washed with methanol (100 ml) and dried to give 5-hydroxy-4-(N-phenyliminomethyl)-1H-indazole (32 g) as a yellow solid. The solid was dissolved in hydrochloric acid (5 M; 500 ml) and heated at 50-60° C. with stirring for 2 hours. The mixture was diluted with water (500 ml) and extracted with ethyl acetate (2×500 ml). The combined extracts were washed with water (500 ml), dried over magnesium sulphate and the solvent evaporated under reduced pressure to give 5-hydroxy-1H-indazole-4-carboxaldehyde (15.48 g) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353002B2
Quelldatensatzuspto-grants-2002_03
ORD IDord-134e0abbe2a841b8868db4b31880a163
Quellennotizuspto-grants-2002_03