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HRID 856683作成日:2026年10月26日

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

https://huagongshe.com/reaction/856683

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EthanolHCID 702—
生成物4-Ethoxypyridine n-oxideHCID 25247999%

反応条件

温度50 °C

反応手順

4-nitropyridine-N-oxide (12 g) was dissolved in ethanol, sodium ethoxide (8.8 g) was added to the mixture, and the mixture was stirred for 40 hours at 50° C. After allowing the mixture to be cooled to room temperature, the precipitates were filtered, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give 4-ethoxypyridine-N-oxide (11.8 g). To 4-ethoxypyridine-N-oxide (11.8 g) was added dimethyl sulfate (8.56 ml), and the mixture was stirred for 1 hour at 110° C. After diluting with methanol (180 ml), the mixture was heated to reflux for 1 hour, an aqueous solution (18 ml) of ammonium peroxodisulfate (20.6 g) was added dropwise to the solution under heat reflux, and the mixture was heated to reflux for 1 hour. After allowing the mixture to be cooled to room temperature, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give (4-ethoxy-2-pyridinyl)methanol (2.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07262185B2
出典データセットuspto-grants-2007_08
ORD IDord-ea5cc24d7f8e45ab98589abaa1ff7bc6
出典メモuspto-grants-2007_08