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

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).

1. customThe solvent was removed under reduced pressure
2. dissolutionthe obtained residue was dissolved in methanol
3. additionan aqueous solution (6.8 ml) of ammonium peroxodisulfate (1.54 g) was added
4. temperatureunder heat
5. temperaturereflux
6. additionAn aqueous solution (3.4 ml) of ammonium peroxodisulfate (0.77 g) was further added to the mixture after 30 minutes
7. stirringthe mixture was stirred for 1 hour
8. temperatureto be cooled to room temperature
9. customthe solvent was removed under reduced pressure
10. customthe obtained residue was purified by silica gel column chromatography

ORD record

ord-fcfad3eb9f514b6b93e4e0d6044f8814

Source dataset

uspto-grants-2007_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07262185B2