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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576750Generated: October 30, 2026

Iodine → HCID 90197331, compound

https://huagongshe.com/reaction/576750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium cerium-nitrateHCID 57418452—
ReactantHCID 86723841HCID 86723841—
SolventAcetonitrileHCID 6342—
ProductHCID 90197331HCID 90197331160.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 1-(3-(trifluoromethyl)phenyl)pyrimidin-2,4(1H,3H)-dione (prepared in Reference Example 113) (5.09 g) in acetonitrile (75 ml) were added iodine (3.03 g) and cerium ammonium nitrate (6.54 g) and the resulting mixture was stirred at 80° C. for thirty minutes. The resulting mixture was cooled to 0° C. and thereto were then added ethyl acetate (150 ml), saturated saline (50 ml) and 5% sodium hydrogen sulfite solution (100 ml) so as to separate the layer. Furthermore, the aqueous layer was extracted with ethyl acetate, and the organic layer was washed with 5% aqueous sodium hydrogen sulfite solution and saturated saline. The resulting mixture was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. To the residue were added ethyl acetate (50 ml) and hexane (100 ml) and the resulting mixture was stirred for fifteen minutes, and the precipitated solids were then collected by filtration and washed with hexane to afford 5-iodo-1-(3-(trifluoromethyl)phenyl)pyrimidin-2,4(1H,3H)-dione (7.34 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040516B2
Source datasetuspto-grants-2015_05
ORD IDord-8afe8595f15e41f890046e2cae0f83a5
Source noteuspto-grants-2015_05