Methane → 2-Chloro-6-methylpyridin-3-ol

5-Hydroxy-2-methylpyridine (1-014-01) (27.01 g) was dissolved in conc. hydrochloric acid (200 mL) and to the reaction mixture was bubbled chlorine gass at 68 to 74° C. After the reaction mixture was stood overnight, the volatile was removed by bubbling nitrogen gas. The reaction mixture was evaporated under reduced pressure to give the crystal residue. The crystal residue was dissolved in methanol, and treated with active charcoal. After recrystallization, the desired 2-chloro-3-hyroxy-6-methylpyridine (1-014-02) (23.96 g, 67.3%) was obtained.

1. customwas bubbled chlorine gass at 68 to 74° C
2. customthe volatile was removed
3. customby bubbling nitrogen gas
4. customThe reaction mixture was evaporated under reduced pressure
5. customto give the crystal residue
6. customAfter recrystallization

ORD-Eintrag

ord-2b07074f87f74c3fa762d2f57ac48cfd

Quelldatensatz

uspto-grants-2005_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06977266B2