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HRID 1050132作成日:2026年10月27日

4-Nitropyridine N-oxide → 4-Ethoxypyridine n-oxide

https://huagongshe.com/reaction/1050132

反応式

関与物質

役割名称HCID仕込み量
反応物4-Nitropyridine N-oxideHCID 14300—
反応物Sodium ethoxideHCID 2723922—
溶媒TetrahydrofuranHCID 8028—
生成物4-Ethoxypyridine n-oxideHCID 25247950.5%

反応条件

温度25 °C

反応手順

To a mixture of 4-nitropyridine 1-oxide (28 g, 200 mmol) in THF (50 mL) was added sodium ethanolate (40.8 g, 600 mmol). The mixture was stirred at 25° C. for 16 h. The reaction residue was then concentrated and the crude material was purified by silica column chromatography (DCM/MeOH=25:1). All fractions found to contain product by TLC (DCM/MeOH=25:1, Rf=0.6) were combined and concentrated to yield a dark red solid of 4-ethoxypyridine 1-oxide (20 g, 101 mmol, 50% yield). 1H NMR (400 MHz, MeOH-d4) δ 8.20 (d, J=7.6 Hz, 2H), 7.12 (d, J=7.6 Hz, 2H), 4.18 (q, J=7.2 Hz, 2H), 1.42 (t, J=6.8 Hz, 3H); ES-LCMS m/z: 140.0 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09382238B2
出典データセットuspto-grants-2016_07
ORD IDord-31c22387772a4f13a13992594843d037
出典メモuspto-grants-2016_07