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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464595Generated: October 31, 2026

Propargyl alcohol → 3-(4-methoxyphenyl)prop-2-yn-1-ol

https://huagongshe.com/reaction/1464595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantDiethylamineHCID 8021—
Reactant4-IodoanisoleHCID 69676—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-(4-methoxyphenyl)prop-2-yn-1-olHCID 1200319194.8%

Reaction Steps

Diethylamine (80 mL, propargyl alcohol (6.4 mL, 0.11 mol), copper(I)iodide (0.7 g), tetrahydrofuran (25 mL), and tetrakis(triphenylphosphine)palladium(o) (1.2 g) were placed in a 250-mL flask under nitrogen. A solution of p-iodoanisole (23.4 g, 0.1 mol) in 40 mL of tetrahydrofuran was added to the reaction dropwise over 30 minutes. The reaction was stirred for 16 hours at room temperature, then evaporated in vacuo to give a dark brown residue. The residue was dissolved in 200 mL of water and extracted four times with diethyl ether (200 mL). The combined extracts were dried over anhydrous sodium sulfate and evaporated to give a dark brown solid that was purified by column chromatography (silica gel), eluting with 9:1 hexane-ethyl acetate to give 15.38 g of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306718
Source datasetuspto-grants-1994_04
ORD IDord-effc7818d44b4bbfaa39cb844d6e89c4
Source noteuspto-grants-1994_04