HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Acetamido-4-methyl-6-benzyloxypyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Amino-4-methyl-6-benzyloxypyrimidine | HCID 23349892 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Acetamido-4-methyl-6-benzyloxypyrimidine | HCID 23349913 | — |
Reaction Steps
Acetic anhydride (15.3 g., 0.15 mole) is added to a stirred suspension of 2-amino-4-methyl-6-benzyloxypyrimidine (23.6 g., 0.11 mole) in 150 ml of benzene. The mixture is heated at reflux for 4 hours. It is cooled, neutralized with aqueous sodium carbonate and the benzene layer separated. The benzene solution is concentrated under vacuum to an oil from which 2-acetamido-4-methyl-6-benzyloxy-pyrimidine melting at 121°-122° C. is isolated by crystallization from hexane n-butyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144338 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-bc2b91c6c4274b16904506d5dd8b9540 |
| Source note | uspto-grants-1979_03 |