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HRID 990182作成日:2026年10月25日

2-(4-Chloro-2-methyl-phenoxy)-3-methyl-5-nitropyridine → 2-(4-Chloro-2-methyl-phenoxy)-3-methyl-5-amino-pyridine

https://huagongshe.com/reaction/990182

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Chloro-2-methyl-phenoxy)-3-methyl-5-nitropyridineHCID 18419461—
反応物HCID 178418361HCID 178418361—
触媒Palladium hydroxideHCID 9942167—
溶媒EthanolHCID 702—
生成物2-(4-Chloro-2-methyl-phenoxy)-3-methyl-5-amino-pyridineHCID 15887616—

反応手順

2-(4-chloro-2-methyl-phenoxy)-3-methyl-5-nitropyridine (5.8 g, 20.8 mmol) was dissolved in 95% ethanol (50 mL) and treated with 20% palladium hydroxide on carbon (350 mg). The reaction mixture was shaken in a hydrogen atmosphere (40 psi) for 1 hour. The solution was filtered through celite and concentrated in vacuo followed by chromatography on SiO2 using 1:1 ethyl acetate/hexanes as eluant. MS (m/z): 248/250 (M+H)+ C13H13N2OCl requires 248.7.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06458813B1
出典データセットuspto-grants-2002_10
ORD IDord-ed6a391318064218bd5915bdf952ebc7
出典メモuspto-grants-2002_10