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HRID 1995821作成日:2026年10月25日

5-[(4-Chlorophenyl)methoxy]-2-nitropyridine → 5-[(4-Chlorophenyl)methoxy]pyridin-2-amine

https://huagongshe.com/reaction/1995821

反応式

関与物質

役割名称HCID仕込み量
反応物5-[(4-Chlorophenyl)methoxy]-2-nitropyridineHCID 20486129—
触媒WaterHCID 962—
溶媒MethanolHCID 887—
生成物5-[(4-Chlorophenyl)methoxy]pyridin-2-amineHCID 20486112—

反応手順

A mixture of 5-(4-chlorobenzyloxy)-2-nitropyridine (0.5 g), Na2S (0.25 g) and methanol (12 ml) is heated to reflux for about 3 hours. Then, a few drops of water is added and refluxing continued about 15 hours. After cooling, the reaction is diluted with methanol, filtered through celite and stripped. The concentrate is taken up in CHCl3, washed with water, dried and stripped giving 2-amino-5-(4-chlorobenzyloxy)pyridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04406690
出典データセットuspto-grants-1983_09
ORD IDord-a45c41810db74af795ff44402984949c
出典メモuspto-grants-1983_09