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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735324Generated: November 3, 2026

Triethylamine → 4-[3,5-Di(trifluoromethyl)phenylethynyl]cyclohexanone

https://huagongshe.com/reaction/1735324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Iodo-3,5-bis(trifluoromethyl)benzeneHCID 630970—
Reactant8-Ethynyl-1,4-dioxaspiro[4.5]decaneHCID 19705273—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product4-[3,5-Di(trifluoromethyl)phenylethynyl]cyclohexanoneHCID 19705254—

Reaction Steps

A solution of 3.9 grams (0.022 mole) of 8-ethynyl-1,4-dioxaspiro[4.5]decane, 10.5 grams (0.031 mole) of 3,5-di(trifluoromethyl)phenyl iodide (prepared in Step A of this Example), 10.7 grams (0.077 mole) of triethylamine, 0.5 gram (catalyst) of bis(triphenylphosphine)palladium(II) chloride, and 0.5 gram (catalyst) of copper(I) iodide in 100 mL of acetonitrile is stirred at ambient temperature for about 18 hours. After this time the reaction mixture is concentrated under reduced pressure to a residue. The residue is then stirred for about 2 hours with 150 mL of aqueous 1N hydrochloric acid. After this time the mixture is extracted with three 100 mL portions of ethyl acetate. The combined extracts are washed with an aqueous solution of 10% lithium chloride. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 4-[3,5-di(trifluoromethyl)phenylethynyl]cyclohexanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536725
Source datasetuspto-grants-1996_07
ORD IDord-b880d0f8758b429eb3e32cd620f49c72
Source noteuspto-grants-1996_07