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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13231Erstellt: 24. Oktober 2026

Dichloromethane → 2-Ethynyl-4-methyl-phenol

https://huagongshe.com/de/reaction/13231

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt2-Bromo-4-methylphenolHCID 23109—
EduktTrimethylsilylacetyleneHCID 66111—
EduktPotassium FluorideHCID 522689—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelHCID 68453242HCID 68453242—
Produkt2-Ethynyl-4-methyl-phenolHCID 10486892—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728051B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-05b116f3a02a429f932af61225491e18
Quellennotizuspto-grants-2010_06