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HRID 1904886作成日:2026年10月27日

Benzamide, N-(5-chloro-2-hydroxy-4-nitrophenyl)- → Benzamide, N-(4-amino-5-chloro-2-hydroxyphenyl)-

https://huagongshe.com/reaction/1904886

反応式

関与物質

役割名称HCID仕込み量
反応物Benzamide, N-(5-chloro-2-hydroxy-4-nitrophenyl)-HCID 5483228—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Benzamide, N-(4-amino-5-chloro-2-hydroxyphenyl)-HCID 78779—

反応手順

In 100 ml of ethanol was dissolved 28 g (96×10-3 mole) of 2-benzamido-4-chloro-5-nitrophenol and hydrogenation was effected by using 1.5 g of Pd-C as a catalyst. The color of the nitro derivative disappeared in 2 hours, and the Pd-C was removed by filtration and ethanol was evaporated from the filtrate, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. 26 g of the crude product was used as such for the following reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04840883
出典データセットuspto-grants-1989_06
ORD IDord-65598d31e3154819a861ae1e3f47c46f
出典メモuspto-grants-1989_06