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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532053Generated: October 26, 2026

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

https://huagongshe.com/reaction/1532053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indazol-5-olHCID 101438—
ReactantMethanimidic acid, N-phenyl-, ethyl esterHCID 111236—
SolventEthanolHCID 702—
Product5-hydroxy-4-(N-phenyliminomethyl)-1H-indazoleHCID 13558159763.5%

Reaction Conditions

Temperature175 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06201004B1
Source datasetuspto-grants-2001_03
ORD IDord-96681f8880224ff0b3375d5256c0f7b5
Source noteuspto-grants-2001_03