Benzyl Bromide → HCID 178517714, compound

To a stirred solution of potassium hydroxide (2.52 g, 45.00 mmol) in methanol (30 mL), was added pyridine-2,3-diol (5.00 g, 45.0 mmol) in 3 portions and a clear red solution was obtained. To this clear red solution was added benzyl bromide (7.70 g, 5.35 mL, 45.00 mmol). The reaction mixture was kept stirring at ambient temperature for 30 minutes, then at 40° C. for 2 hours. The solvent was removed in vacuo and the residue was dissolved in dichloromethane (100 mL), and washed with water (100 mL). The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo. The residue was recrystallized from methanol (20 mL) to afford the title compound (4.60 g, 51%): 1H NMR (300 MHz, DMSO-d6) δ 11.63 (s, 1H), 7.44-7.33 (m, 5H), 6.96-6.88 (m, 2H), 6.07 (t, J=6.0 Hz, 1H), 5.00 (s, 2H); MS (ES+) m/z 202.2 (M+1).

1. customa clear red solution was obtained
2. waitat 40° C. for 2 hours
3. customThe solvent was removed in vacuo
4. dissolutionthe residue was dissolved in dichloromethane (100 mL)
5. washwashed with water (100 mL)
6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
7. filtrationfiltered
8. concentrationThe filtrate was concentrated in vacuo
9. customThe residue was recrystallized from methanol (20 mL)

ORD record

ord-5620016b75cc4bf09d10cc2439576b1b

Source dataset

uspto-grants-2013_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08501746B2