HuagongsheHuagongshe Chemistry Print Report · For research reference only
Peracetic Acid → HCID 178502003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Methyl 2-amino-6-[(p-tolylsulfonyl)oxy]-4-pyrimidinecarbamate | HCID 12857764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178502003 | HCID 178502003 | — |
Reaction Steps
6.75 ml of 40% peracetic acid are added dropwise at 0° to a suspension of 3.4 g (10 mmol) of methyl 2-amino-6-([p-toluenesulfonyl)oxy]-4-pyrimidinecarbamate in 120 ml of absolute ethanol. The mixture is stirred at room temperature for 48 hours and thereafter poured into an aqueous solution of sodium sulfite. Ethyl acetate is added thereto, the organic phase is separated, dried over sodium sulphate and evaporated under reduced pressure. The residue is recrystallized from methylene chloride/methanol, there being obtained methyl 2-amino-6-[(p-toluenesulfonyl)oxy]-4-pyrimidinecarbamate-3-oxide of melting point 144°-145°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04549019 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-e04ecc0b849b4f82b5f2ecf9414c4f2a |
| Source note | uspto-grants-1985_10 |