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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantN-IodosuccinimideHCID 120273—
Reactant1,3-Dimethyl-6-(trifluoromethyl)uracilHCID 2758669—
Reactantsodium thiosulfite anhydrousHCID 15847209—
SolventPotassium CarbonateHCID 11430—
Product1,3-Dimethyl-5-iodo-6-(trifluoromethyl)uracilHCID 2261371466%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380387B1
Source datasetuspto-grants-2002_04
ORD IDord-93837f21262b4ec49dfe9dd9dc9a902d
Source noteuspto-grants-2002_04