HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(6-bromopyridin-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Amino-6-bromopyridine | HCID 300809 | — |
| Product | N-(6-bromopyridin-2-yl)acetamide | HCID 10353221 | 68% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04211871 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-6d15efdf57654e1485bfd53d1440be9a |
| Source note | uspto-grants-1980_07 |