Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Uracil | HCID 1174 | — |
| Reactant | Trifluoroiodomethane | HCID 16843 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Catalyst | Iron(II) tetrafluoroborate | HCID 11736352 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Trifluoromethyluracil | HCID 5899 | 94% |
Reaction Steps
0.11 g (1.0 mmol) of uracil was weighed and placed in a 50 ml two-neck flask equipped with a magnetic rotor and the atmosphere in the flask was replaced with argon. The following materials were added thereinto: 0.21 ml of a 42% tetrafluoroboric acid aqueous solution, 2.0 ml of dimethyl sulfoxide, 3.0 ml of a 2.0 mol/l dimethyl sulfoxide solution of trifluoromethyl iodide, 0.3 ml of a 1.0 mol/l aqueous solution of iron (II) tetrafluoroborate and 0.2 ml of a 30% hydrogen peroxide aqueous solution. The mixture was stirred at 40 to 50° C. for 20 minutes and then the resulting solution was cooled to room temperature. Formation of 5-trifluoromethyluracil (19F-NMR yield: 94%) was confirmed in the same manner as in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884202B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-30bdf16ae7bc437a80c962aa88627011 |
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| Source note | uspto-grants-2011_02 |
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