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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735932Generated: October 25, 2026

Triethylamine → 4-[(4-Hexylphenyl)ethynyl]benzaldehyde

https://huagongshe.com/reaction/735932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant1-Ethynyl-4-hexylbenzeneHCID 2775129—
CatalystTriphenylphosphineHCID 11776—
Catalystcopper(I) bromideHCID 24593—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product4-[(4-Hexylphenyl)ethynyl]benzaldehydeHCID 1128928698.6%

Reaction Steps

A mixture of 4-bromobenzaldehyde (5.00 g, 27.0 mmol), 1-ethynyl-4-hexylbenzene (6.29 g, 33.4 mmol), Et3N (4.70 mL, 33.4 mmol), bis(triphenylphosphine)palladium chloride (950 mg, 1.35 mmol) and triphenylphosphine (180 mg, 0.68 mmol) in anhydrous THF (100 mL) was stirred at rt for 30 min under inert atmosphere. Then copper(I) bromide (82 mg, 0.43 mmol) was added and the resulting mixture was stirred overnight at rt. The solvent was evaporated off. The residue was dissolved in Et2O (100 mL), washed with water (50 mL), dried over MgSO4 and the solvent was removed under reduced pressure. The resulting brown solid was triturated in hexane (25 mL), filtered off and washed with hexane to give the title compound as a beige solid (7.73 g, 91%). HPLC (Condition A), Rt: 5.88 min (HPLC purity: 91.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592477B2
Source datasetuspto-grants-2009_09
ORD IDord-c5bbc70b54144cd691e27e94c5b42525
Source noteuspto-grants-2009_09