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HRID 856678作成日:2026年10月27日

4-chloropyridine N-oxide → (4-Chloropyridin-2-yl)methanol

https://huagongshe.com/reaction/856678

反応式

関与物質

役割名称HCID仕込み量
反応物4-chloropyridine N-oxideHCID 70724—
反応物Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
溶媒DichloromethaneHCID 6344—
生成物(4-Chloropyridin-2-yl)methanolHCID 276316761.8%

反応手順

4-chloropyridine-N-oxide (4.4 g) was dissolved in methylene chloride (68 ml), trimethyloxonium tetrafluoroborate (5.0 g) was added to the mixture, and the mixture was stirred for 90 minutes at room temperature. The solvent was removed under reduced pressure, the obtained residue was dissolved in methanol, and an aqueous solution (6.8 ml) of ammonium peroxodisulfate (1.54 g) was added thereto under heat reflux. An aqueous solution (3.4 ml) of ammonium peroxodisulfate (0.77 g) was further added to the mixture after 30 minutes, the mixture was stirred 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-chloro-2-pyridinyl)methanol (3.0 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-fcfad3eb9f514b6b93e4e0d6044f8814
出典メモuspto-grants-2007_08