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HRID 1398774作成日:2026年10月27日

Ammonium Chloride → 2-Methoxy-4-methyl-5-nitropyridine

https://huagongshe.com/reaction/1398774

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2-Chloro-4-methyl-5-nitropyridineHCID 345364—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
生成物2-Methoxy-4-methyl-5-nitropyridineHCID 24316998%

反応手順

A solution of 2-chloro-4-methyl-5-nitropyridine (3.0 g, 17.3 mmol) in methanol (20 mL) was added a solution of sodium methoxide (28% in methanol, 10 mL) dropwise at 0° C. The mixture was warmed to room temperature and stirred for 16 hr. The mixture was neutralized by addition of aqueous ammonium chloride and concentrated in vacuo. The residue was dissolved in water and extracted with ethyl acetate. Organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to give the title compound (2.84 g, 16.8 mmol, 98%) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08901141B2
出典データセットuspto-grants-2014_12
ORD IDord-5af145c853f74bec9de396d8d7a0df88
出典メモuspto-grants-2014_12