HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21436690, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Chloro-3-nitropyridin-2-amine | HCID 4071694 | — |
| Product | HCID 21436690 | HCID 21436690 | — |
Reaction Steps
When 10.0 g. of 4-chloro-2-amino-3-nitropyridine, from Example I-5, and 20 ml of acetic anhydride are heated under reflux for 1 hour and then concentrated, there is obtained 2-acetamido-4-chloro-3-nitropyridine, and, this, heated at 300° C. and treated with chlorine gives 2-acetamido-4,5-dichloro-3-nitropyridine. The latter by the procedure of Example I-2 gives 2-amino-4,5-dichloro-3-pyridinol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022897 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-bfdc0f89e37545c7bfd516aaa44c0a3a |
| Source note | uspto-grants-1977_05 |