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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505831Generated: October 27, 2026

Dichloromethane → 331735-28-5

https://huagongshe.com/reaction/505831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-(4-Bromophenyl)ethanolHCID 72851—
ReactantPotassium FluorideHCID 522689—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDioxan triethylamineHCID 68453242—
Product331735-28-5HCID 57577839—

Reaction Steps

A flask is flushed with N2 and charged with 4-bromo-phenethyl alcohol (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 solvent is 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 is 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-(4-ethynyl-phenyl)-ethanol (2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781571B2
Source datasetuspto-grants-2010_08
ORD IDord-0ccc2ad36c5c442b9fa4c3580aa3be9c
Source noteuspto-grants-2010_08