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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363443Generated: October 26, 2026

Hydrogen Peroxide → 6-Carboxy-5-trifluoromethyluracil

https://huagongshe.com/reaction/1363443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantOrotic AcidHCID 967—
ReactantSulfuric AcidHCID 1118—
ReactantTrifluoroiodomethaneHCID 16843—
CatalystBis(eta-cyclopentadienyl) ironHCID 7611—
SolventDimethyl SulfoxideHCID 679—
Product6-Carboxy-5-trifluoromethyluracilHCID 5769342995%

Reaction Conditions

Temperature65 °C

Reaction Steps

0.17 g (1.0 mmol) of 6-carboxyuracil and 0.058 g (0.3 mmol) of ferrocene were 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: 1.8 ml of dimethyl sulfoxide, 2.0 ml of a 1N dimethyl sulfoxide solution of sulfuric acid, 1.0 ml of a 3.0 mol/l dimethyl sulfoxide solution of trifluoromethyl iodide and 0.2 ml of a 30% hydrogen peroxide aqueous solution. The mixture was stirred at 60 to 70° C. for 20 minutes and then the resulting solution was cooled to room temperature. Formation of 6-carboxy-5-trifluoromethyluracil (19F-NMR yield: 95%) was confirmed by 19F-NMR with 2,2,2-trifluoroethanol as an internal standard. 6-Carboxy-5-trifluoromethyluracil was obtained (0.076 g, yield: 34%) by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884202B2
Source datasetuspto-grants-2011_02
ORD IDord-688cd5ea4ab14455a49b9fa2df9f65ea
Source noteuspto-grants-2011_02