HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464784Generated: October 29, 2026
m-Chloroperbenzoic acid → HCID 178502003, compound
https://huagongshe.com/reaction/464784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Methyl 2-amino-6-[(p-tolylsulfonyl)oxy]-4-pyrimidinecarbamate | HCID 12857764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178502003 | HCID 178502003 | — |
Reaction Steps
350 g of methyl 2-amino-6-[(p-tolylsulfonyl)oxy]-4-pyrimidinecarbamate are suspended in 6.3 l of methylene chloride and 1 l of methanol. At room temperature there are added thereto 370 g of m-chloroperbenzoic acid and the mixture is stirred for a further 16 hours. The yellowish solution is subsequently extracted with 3 l of 2N soda solution. The aqueous phase is extracted with 1 l of methylene chloride. The combined organic phases are washed with 2 l of water and evaporated in vacuo. The crystalline residue is suspended in 1.5 l of ether while stirring. The pale yellowish crystals are filtered off under suction and washed with 0.5 l of ether. After drying at 40° in vacuo, there is obtained methyl 2-amino-6-[(p-tolylsulfonyl)oxy]-4-pyrimidinecarbamate-3-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04549019 |
|---|
| Source dataset | uspto-grants-1985_10 |
|---|
| ORD ID | ord-04d4688b5ef24524bd2d281d4d537b31 |
|---|
| Source note | uspto-grants-1985_10 |
|---|