HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990619Generated: November 2, 2026
Ammonium Persulfate → HCID 18415665, compound
https://huagongshe.com/reaction/990619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 12056510 | HCID 12056510 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18415665 | HCID 18415665 | 88% |
Reaction Steps
To a stirred solution of 10.7 g (0.033 mol) 3-(bromodifluoromethylthio)-1-(N,N-diethylcarbamoyl)-1,2,4-triazole, prepared as in Example 1, step (c), in 25 ml N,N-dimethylformamide, was added 4.11 g (0.065 mol) ammonium formate and 2.24 g (0.01 mol) ammonium persulfate and the mixture was heated at 50° C. for 2.5 h. The reaction mixture was then diluted with 100 ml water and extracted with ether (3×100 ml). The combined resulting organic layers were washed with water, dried over MgSO4 and evaporated to give 7.2 g (88% yield) of the desired 1-(N,N-diethylcarbamoyl)-3-(difluoromethylthio)-1,2,4-triazole as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06461997B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-c7c9e0c12671443b87766f1f642371c6 |
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| Source note | uspto-grants-2002_10 |
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