HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(4,6-Dimethoxypyrimidine-2-ylcarbonyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4,6-Dimethoxypyrimidine-2-ylcarbonyl)acetanilide | HCID 17856762 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4,6-Dimethoxypyrimidine-2-ylcarbonyl)aniline | HCID 17856750 | — |
Reaction Steps
In a reactor were placed 0.57 g (1.9 m moles) of 2-(4,6-dimethoxypyrimidine-2-ylcarbonyl)acetanilide, 10 ml of methanol and 5 ml of 6 N hydrochloric acid, followed by refluxing for 1 hour with heating. After the completion of the reaction, the reaction mixture was made alkaline with sodium hydroxide, after which extraction with ethyl acetate was made. The ethyl acetate layer was concentrated. The residue was subjected to gas chromatography. As a result, formation of 2-(4,6-dimethoxypyrimidine-2-ylcarbonyl)aniline was confirmed. Conversion: 100% (in terms of total area ratio in gas chromatography)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504503B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-4fdc6ef40e694658b59d4f1ba023267d |
| Source note | uspto-grants-2009_03 |