HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226106Generated: November 2, 2026
Sodium Trifluoroacetate → HCID 53759503, compound
https://huagongshe.com/reaction/2226106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Trifluoroacetate | HCID 517019 | — |
| Reactant | HCID 18966276 | HCID 18966276 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 53759503 | HCID 53759503 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05346881 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-367455da77ec471f941e0b8c2f4b6a15 |
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| Source note | uspto-grants-1994_09 |
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