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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226106Generated: November 2, 2026

Sodium Trifluoroacetate → HCID 53759503, compound

https://huagongshe.com/reaction/2226106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium TrifluoroacetateHCID 517019—
ReactantHCID 18966276HCID 18966276—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylacetamideHCID 31374—
ProductHCID 53759503HCID 53759503—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 6.0 g (0.044 mole) of sodium trifluoroacetate, 4.18 g (0.022 mole) of copper(I)iodide, and 40 mL of N,N-dimethylacetamide under a nitrogen atmosphere at 140 ° C is added 4.83 g (0.011 mole) of 3-(7-bromo-2,2-dimethyl-5-fluoro- 1,3-benzodioxol-4-yl)- 1 -methyl-6-trifluoromethyluracil (Example 3). The temperature is then raised to 150° C. at which the reaction mixture is stirred for three hours. After being cooled to ambient temperature, the reaction mixture is poured into ice and then extracted with diethyl ether. The combined extracts are dried over anhydrous magnesium sulfate and filtered. The filtrate is evaporated under reduced pressure, leaving a residue which is purified using column chromatography on silica gel. The product-containing fractions are combined and the solvent evaporated under reduced pressure, leaving 3-(2,2-dimethyl-5-fluoro-7-trifluoromethyl- 1,3-benzodioxol-4-yi)- 1 -methyl-6-trifluoromethyluracil as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346881
Source datasetuspto-grants-1994_09
ORD IDord-367455da77ec471f941e0b8c2f4b6a15
Source noteuspto-grants-1994_09