HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012880Generated: November 1, 2026
Hydrogen Peroxide → HCID 178430911, compound
https://huagongshe.com/reaction/1012880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Methylpyrazole | HCID 3406 | — |
| Reactant | Trifluoroiodomethane | HCID 16843 | — |
| Catalyst | Bis(eta-cyclopentadienyl) iron | HCID 7611 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178430911 | HCID 178430911 | 45% |
Reaction Steps
0.047 g (0.25 mmol) of ferrocene was weighed and placed in a two-neck flask and the atmosphere in the flask was replaced with argon. The following materials were added thereinto: 0.07 ml (0.88 mmol) of 4-methylpyrazole, 1.7 ml of dimethyl sulfoxide, 1.7 ml of a 1 N dimethyl sulfoxide solution of sulfuric acid, 0.7 ml of a 3.0 mol/l dimethyl sulfoxide solution of trifluoromethyl iodide and 0.15 ml of a 30% hydrogen peroxide aqueous solution, and the mixture was stirred for 20 minutes. During the stirring, the temperature of the reaction system rose up in the range of from 40° C. to 50° C. Thereafter the resulting solution was cooled to room temperature. Formation of 4-methyl-3-trifluoromethylpyrazole (19F-NMR yield: 45%) was confirmed by 19F-NMR with 2,2,2-trifluoroethanol as an internal standard. The subsequent procedure was conducted in the same manner as in Example 1 and 4-methyl-3-trifluoromethylpyrazole was obtained as a colorless oil (0.054 g, yield: 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981318B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-26b137f5336d4f379c13945e7cb329c0 |
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| Source note | uspto-grants-2011_07 |
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