Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057261Generated: October 25, 2026

Toluene → 4-[(4-Pentylphenyl)ethynyl]phenol

https://huagongshe.com/reaction/1057261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-IodophenylacetateHCID 141793—
Reactant1-Ethynyl-4-pentylbenzeneHCID 2775131—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDiisopropylamineHCID 7912—
Product4-[(4-Pentylphenyl)ethynyl]phenolHCID 18671138—

Reaction Steps

4-Pentylphenylacetylene (10.5 g, 61.4 mmol), 4-acetoxyphenyl iodide (16.1 g, 61.4 mmol), a catalytic amount of Pd(PPh3)2Cl2 and a catalytic amount of copper iodide were stirred in diisopropylamine (100 ml) at 70° C. After 5 minutes, a precipitate was seen and the mixture became unstirrable, toluene (100 ml) was added. The mixture was stirred at room temperature for 24 hours and then evaporated to dryness on a rotary evaporator. The residue was redissolved in aqueous potassium hydroxide ethanolic solution and stirred at 70° C. overnight. The mixture was evaporated to dryness, then partitioned between ethyl acetate and water, the organic phase was removed, dried and evaporated. The residue was purified by flash column chromatography using DCM as eluant. A pink coloured solid was left after evaporation of the appropriate fractions. Yield=10.4 g, 64%. 1H-NMR and IR spectroscopy gave the expected signals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514578B1
Source datasetuspto-grants-2003_02
ORD IDord-fbc96aea378f44dca8347db3b9ca696d
Source noteuspto-grants-2003_02