HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(2-Chloro-4-methylpyrimidin-5-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Chloro-4-methylpyrimidin-5-amine | HCID 316282 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(2-Chloro-4-methylpyrimidin-5-yl)acetamide | HCID 23070222 | 86.8% |
Reaction Steps
A solution of 2-chloro-4-methylpyrimidin-5-amine (10 g, 68.26 mmol, 1.00 equiv, 98%) and acetic anhydride (14.3 g, 137.27 mmol, 2.01 equiv, 98%) in acetic acid (50 mL) was stirred at room temperature for 2 h. The resulting mixture was concentrated under vacuum to give 11 g (82%) of N-(2-chloro-4-methylpyrimidin-5-yl)acetamide as an off-white solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-2f605f27763d4b8d99de8ab611aca9e8 |
| Source note | uspto-grants-2014_02 |