Hydrogen Bromide → 4-Bromo-2,3-dimethylpyridine 1-oxide

Temperatur

100 °C

A mixture of 2,3-dimethyl-4-nitropyridine N-oxide (5 g, 29.7 mmol) and hydrogen bromide (30% wt in acetic acid, 100 mL) was heated for 48 hours at 100° C. The mixture was then filtered, washing through with 2M sodium hydroxide and the filtrate was extracted with dichloromethane (×3). The combined organic solutions were washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with ethyl acetate:pentane, 50:50, to afford the title product as a pale yellow solid.

1. filtrationThe mixture was then filtered
2. washwashing through with 2M sodium hydroxide
3. extractionthe filtrate was extracted with dichloromethane (×3)
4. washThe combined organic solutions were washed with brine
5. dry with materialdried over sodium sulfate
6. concentrationconcentrated in vacuo
7. customThe residue was purified by column chromatography on silica gel
8. washeluting with ethyl acetate

ORD-Eintrag

ord-d418d361687d4d1393b167dbf84b659b

Quelldatensatz

uspto-grants-2011_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07875615B2