HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868639Generated: October 25, 2026
Hydrogen Peroxide → 1-Acetoxy-6-amino-1,2-dihydro-2-imino-4-(4-toluenesulfonyloxy)pyrimidine
https://huagongshe.com/reaction/868639
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 12661239 | HCID 12661239 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Acetoxy-6-amino-1,2-dihydro-2-imino-4-(4-toluenesulfonyloxy)pyrimidine | HCID 22164170 | — |
Reaction Steps
2.8 g (0.001 mole) of 2,6-diamino-4-tosyloxypyrimidine are added to 70 ml of absolute ethanol. 5 ml of a 70% aqueous hydrogen peroxide solution are added to the obtained suspension at 40° C., then 3 ml of acetic anhydride are added dropwise. The suspension is homogenised by heating to 60° C., and the solution gets slowly opalescent while standing. Tracing the reaction by thin layer chromatography it will be found that the reaction has completed and the aimed compound is accompanied by some diacetyl compound. By filtering the reaction mixture 0.35 g of a solid material is separated. If the ethyl alcohol is distilled off and the residue is allowed to stand in a refrigerator, no product separation can be observed. Of decanting the water and dissolving the residue in ethanol a crystalline product is obtained. In this way 1.95 g (54%) of the aimed compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04780537 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-ee61d2b4999d42c59e3023196be5d79d |
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| Source note | uspto-grants-1988_10 |
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