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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978848Generated: October 26, 2026

Water → 3-[4-Chloro-3-(2-(2,2,2-trifluoroethoxycarbonyl)-ethenyl)-phenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine

https://huagongshe.com/reaction/1978848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,2,2-Trifluoroethyl acrylateHCID 67889—
ReactantSodium AcetateHCID 517045—
Reactant3-[4-Chloro-3-iodophenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidineHCID 21201234—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product3-[4-Chloro-3-(2-(2,2,2-trifluoroethoxycarbonyl)-ethenyl)-phenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidineHCID 86583794—

Reaction Conditions

Temperature120 °C

Reaction Steps

A suspension of 5.0 g of 3-[4-chloro-3-iodophenyl]-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine, 2.0 g of 2,2,2-trifluoroethyl acrylate, 0.5 mg of palladium acetate and 1.1 g of sodium acetate in 50 ml of dimethylformamide was stirred for 4 hours at 120° C., after which further palladium acetate and 2,2,2-trifluoromethyl acrylate were added and stirring was continued for a further 2 hours at 120° C. The cooled reaction mixture was added to 200 ml of water and the precipitate was isolated, washed with petroleum ether and dried under greatly reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239074B1
Source datasetuspto-grants-2001_05
ORD IDord-6ae1bdc470bb4dc3b04ffbb8d23cdc90
Source noteuspto-grants-2001_05