Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503100Generated: October 31, 2026

Potassium Iodide → N-(5,5-diethoxy-1,1,1-trifluoro-pent-3-yn-2-ylidene)-4-methoxyaniline

https://huagongshe.com/reaction/1503100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3,3-DiethoxypropyneHCID 66285—
Reactant2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl ChlorideHCID 10421682—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-(5,5-diethoxy-1,1,1-trifluoro-pent-3-yn-2-ylidene)-4-methoxyanilineHCID 86723351—

Reaction Conditions

Temperature60 °C

Reaction Steps

In a typical reaction, 2,2,2-trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride and a slight excess of 3,3-diethoxyprop-1-yne are mixed with about 0.3 equivalents of copper (I) iodide and slight excesses of potassium phosphate and potassium iodide in anhydrous acetonitrile. The mixture is heated at about 60° C. under a nitrogen atmosphere until the reaction is complete. After cooling, an extraction solvent like a halogenated hydrocarbon is added to the mixture along with water. The organic layer is recovered, washed with brine and dried. The solvent is evaporated to provide crude N-(5,5-diethoxy-1,1,1-trifluoro-pent-3-yn-2-ylidene)-4-methoxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212141B2
Source datasetuspto-grants-2015_12
ORD IDord-29a1babea8234771aa4f00185501d85f
Source noteuspto-grants-2015_12