Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13231Generated: October 26, 2026

Dichloromethane → 2-Ethynyl-4-methyl-phenol

https://huagongshe.com/reaction/13231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-Bromo-4-methylphenolHCID 23109—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantPotassium FluorideHCID 522689—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventHCID 68453242HCID 68453242—
Product2-Ethynyl-4-methyl-phenolHCID 10486892—

Reaction Steps

A flask is flushed with N2 and charged with 2-Bromo-4-methylphenol (20 mmol) and dissolved in 1/1 Et3N/dioxane. Bis(triphenylphosphine)palladium(II) dichloride (PdCl2(PPh3)2) (0.2 mmol) is added, followed by 0.4 mmol of CuI. Trimethylsilylacetylene (24 mmol) is added drop-wise to the reaction mixture. The reaction mixture is stirred overnight under N2. The solvents are removed under vacuum and the resulting liquid is extracted by washing with ethyl ether. The ethyl ether extracts are combined and washed with H2O, then dried over anhydrous sodium sulfate. The solvent was removed under vacuum and the product is purified by column chromatography. The purified product is placed in a N2-flushed flask and dissolved in methanol. Potassium fluoride (65 mmol) is added and the reaction stirred under a N2 blanket for 16 h. The reaction mixture is poured into CH2Cl2 and extracted with H2O, then dried over Na2SO4, filtered and the solvent is removed under vacuum. The resulting product is purified by column chromatography to yield 2-ethynyl-4-methyl-phenol (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728051B2
Source datasetuspto-grants-2010_06
ORD IDord-05b116f3a02a429f932af61225491e18
Source noteuspto-grants-2010_06