Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Deoxyuridine | HCID 13712 | — |
| Reactant | Trifluoroiodomethane | HCID 16843 | — |
| Catalyst | Ferrous Sulfate | HCID 24393 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Trifluridine | HCID 6256 | 85% |
Reaction Steps
0.23 g (1.0 mmol) of 2′-deoxyuridine 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: 2.0 ml of a 1N dimethyl sulfoxide solution of sulfuric acid, 1.0 ml of a 2.1 mol/l dimethyl sulfoxide solution of trifluoromethyl iodide, 0.2 ml of a 30% hydrogen peroxide aqueous solution and 0.3 ml of a 1.0 mol/l aqueous solution of iron (II) sulfate. 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-trifluoromethyl-2′-deoxyuridine (19F-NMR yield: 85%) was confirmed by 19F-NMR with 2,2,2-trifluoroethanol as an internal standard. 5-Trifluoromethyl-2′-deoxyuridine was obtained as a white solid (0.17 g, yield: 58%) by column chromatography.
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-e455fd15a0244ff3ab57923ceedd8d1e |
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| Source note | uspto-grants-2011_02 |
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