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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727190Generated: October 30, 2026

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

https://huagongshe.com/reaction/727190

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 numberUS05712281
Source datasetuspto-grants-1998_01
ORD IDord-490946760c004400add7ed9f518badf6
Source noteuspto-grants-1998_01