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HRID 1921286作成日:2026年10月27日

N-(4-methyl-3-nitrophenyl)cyclopropanecarboxamide → N-(3-amino-4-methylphenyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/1921286

反応式

関与物質

役割名称HCID仕込み量
反応物N-(4-methyl-3-nitrophenyl)cyclopropanecarboxamideHCID 4104437—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物N-(3-amino-4-methylphenyl)cyclopropanecarboxamideHCID 2469353794.8%

反応手順

N-(4-Methyl-3-nitrophenyl)cyclopropanecarboxamide (409 mg) was hydrogenated over 10% Pd/C (50% wet, 80 mg) at atmospheric pressure of hydrogen in MeOH (20 mL) for 5 hr. The catalyst was removed by filtration through Celite® pad and the filtrate was evaporated in vacuo to give N-(3-amino-4-methylphenyl)cyclopropanecarboxamide (335 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173684B2
出典データセットuspto-grants-2012_05
ORD IDord-1148f2f8c34e49a9a37dc682729e6a91
出典メモuspto-grants-2012_05