Acetic Anhydride → N-(6-bromopyridin-2-yl)acetamide
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Br:8])[N:3]=1.[C:9](OC(=O)C)(=[O:11])[CH3:10]>>[C:9]([NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Br:8])[N:3]=1)(=[O:11])[CH3:10]Participants
3
Procedure
20 g (0.116 mole) of 2-amino-6-bromopyridine was dissolved in 140 ml. acetic anhydride and heated at 70° C. for 45 minutes. 2-Acetamido-6-bromopyridine was isolated by filtration as white flakes, m.p=159.2°-160.0° C., in 68% yield. The excess acetic anhydride present in the reaction mixture was hydrolyzed by the addition of 300 ml. water to the filtrate; the reaction mixture was agitated and an additional 27% yield of 2-acetamido-6-bromopyridine was collected by filtration, giving a 95% yield of reaction product, 2-acetamido-6-bromopyridine which was recrystallized from benzene.
Sources & evidence
- ORD record
- ord-6d15efdf57654e1485bfd53d1440be9a
- Source dataset
- uspto-grants-1980_07
- Patent number
- US04211871
Reaction notes
Loading…