HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[(2-Chloropyridin-4-YL)methyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Chloro-4-cyanopyridine | HCID 568638 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-[(2-Chloropyridin-4-YL)methyl]acetamide | HCID 15079268 | — |
Reaction Steps
A mixture of 2-chloro-4-cyanopyridine (1.9 g), platinum dioxide (0.3 g), acetic anhydride (50 ml) and acetic acid (50 ml) was stirred under an atmosphere of hydrogen for 2 hours. The mixture was filtered and the filtrate was evaporated. The residue was partitioned between chloroform and dilute aqueous sodium bicarbonate solution. The organic phase was dried (MgSO4) and evaporated to give N-(2-chloropyrid-4-ylmethyl)acetamide (1.5 g), as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05252573 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-094f8bf3d0fd4d3f8bf5e7d7f7c16df8 |
| Source note | uspto-grants-1993_10 |