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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464784Generated: October 29, 2026

m-Chloroperbenzoic acid → HCID 178502003, compound

https://huagongshe.com/reaction/464784

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl 2-amino-6-[(p-tolylsulfonyl)oxy]-4-pyrimidinecarbamateHCID 12857764—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178502003HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04549019
Source datasetuspto-grants-1985_10
ORD IDord-04d4688b5ef24524bd2d281d4d537b31
Source noteuspto-grants-1985_10