Methanol → Methyl 3-bromoisonicotinate

H2SO4 (2.5 mL, 48.3 mmol, 1.0 eq.) was added to a solution of 3-bromoisonicotinic acid (9.7 g, 48.3 mmol, 1.0 eq.) in MeOH (150 mL). The resulting solution was stirred for 14 hours while the temperature was maintained at reflux in an oil bath. The mixture was then cooled to room temperature and concentrated under vacuum. The residue was dissolved in EtOAc (200 mL). The pH of the solution was adjusted to 10 with Na2CO3. The resulting solution was extracted with EtOAc (100 mL). The organic layer was washed with water (1×200 mL) and saturated aqueous NaCl (2×100 mL). The mixture was dried over anhydrous Na2SO4 and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with EtOAc/PE (1:20) to yield 3-bromoisonicotinic acid methyl ester (4.4 g) as a colorless liquid.

1. temperaturewas maintained
2. temperatureat reflux in an oil bath
3. concentrationconcentrated under vacuum
4. dissolutionThe residue was dissolved in EtOAc (200 mL)
5. extractionThe resulting solution was extracted with EtOAc (100 mL)
6. washThe organic layer was washed with water (1×200 mL) and saturated aqueous NaCl (2×100 mL)
7. dry with materialThe mixture was dried over anhydrous Na2SO4
8. concentrationconcentrated under vacuum
9. washeluted with EtOAc/PE (1:20)

ORD-Eintrag

ord-bce1e111dcf741eaab7a152d9b77f906

Quelldatensatz

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08530663B2