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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 856678생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/856678

반응식

참여 물질

역할이름HCID투입량
반응물4-chloropyridine N-oxideHCID 70724—
반응물Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
용매DichloromethaneHCID 6344—
생성물(4-Chloropyridin-2-yl)methanolHCID 276316761.8%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07262185B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-fcfad3eb9f514b6b93e4e0d6044f8814
출처 메모uspto-grants-2007_08