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HRID 1771633作成日:2026年10月27日

N-(2,6-dimethyl-3-nitrophenyl)acetamide → N-(3-amino-2,6-dimethylphenyl)acetamide

https://huagongshe.com/reaction/1771633

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2,6-dimethyl-3-nitrophenyl)acetamideHCID 223591—
触媒PalladiumHCID 23938—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
生成物N-(3-amino-2,6-dimethylphenyl)acetamideHCID 84784819.3%

反応手順

N-(2,6-dimethyl-3-nitro-phenyl)acetamide (12 g, 58 mmol, 1.0 eq) was dissolved in a mixture of MeOH (60 mL), EtOH (30 mL) and acetic acid (60 mL). Pd/C (1.6 g, 10%) was added and the reaction stirred at room temperature under H2 for 36 h. The catalyst was removed by filtration through celite and the filtrate collected. Water was added and the pH adjusted to pH 8 by addition of aqueous NaHCO3. The solution was concentrated in vacuo to remove methanol and ethanol. The aqueous layer was extracted with EtOAc and the combined organic extracts were dried (Na2SO4) filtered and evaporated in vacuo. The crude product was purified by column chromatography (EtOAc:petroleum ether, 1:10 to 1:1) to give the title compound as a yellow solid (2 g, 19%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09249085B2
出典データセットuspto-grants-2016_02
ORD IDord-e7bc835ed10c4d12b461dc0aca9f5049
出典メモuspto-grants-2016_02