HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844869Generated: October 25, 2026
Trifluoroacetic acid → 1,3-Dimethyl-5-iodo-6-(trifluoromethyl)uracil
https://huagongshe.com/reaction/844869
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 1,3-Dimethyl-6-(trifluoromethyl)uracil | HCID 2758669 | — |
| Reactant | sodium thiosulfite anhydrous | HCID 15847209 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | 1,3-Dimethyl-5-iodo-6-(trifluoromethyl)uracil | HCID 22613714 | 66% |
Reaction Steps
A mixture of 1,3-dimethyl-6-(trifluoromethyl)uracil (16.91 mmol, 3.52 g), trifluoroacetic acid (20 mL) and trifluoroacetic anhydride (5 mL) was refluxed for 5 min. Then, NIS (16.91 mmol, 3.8 g) was added and the resulting mixture was stirred for 15 h at which time the TLC analysis of the reaction mixture indicated the presence of some starting material. Another portion of NIS (8.45 mmol, 1.9 g) was added and reflux was continued for another 5 h. The reaction mixture was cooled to room temperature and was poured slowly into a saturated potassium carbonate solution (100 mL). Then, sodium thiosulfite solution was added to remove the excess iodine color. The resulting solids were collected by filtration and washed with water. After air drying, 3.73 g (66% yield) of 1,3-dimethyl-5-iodo-6-(trifluoromethyl)uracil was obtained as a white solid: mp 149-151° C. EI-HRMS m/e calcd for C7H6F3IN2O2 (M+) 333.9426, found 333.9436.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380387B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-93837f21262b4ec49dfe9dd9dc9a902d |
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| Source note | uspto-grants-2002_04 |
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