戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 275779作成日:2026年10月26日

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

https://huagongshe.com/reaction/275779

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Indazol-5-olHCID 101438—
反応物Methanimidic acid, N-phenyl-, ethyl esterHCID 111236—
溶媒EthanolHCID 702—
生成物5-hydroxy-4-(N-phenyliminomethyl)-1H-indazoleHCID 13558159763.5%

反応条件

温度175 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353002B2
出典データセットuspto-grants-2002_03
ORD IDord-134e0abbe2a841b8868db4b31880a163
出典メモuspto-grants-2002_03