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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734835Generated: October 30, 2026

Triethylamine → 3-(1-Undecynyl)benzaldehyde

https://huagongshe.com/reaction/1734835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-UndecyneHCID 75249—
Reactant3-BromobenzaldehydeHCID 76583—
CatalystCopper iodideHCID 83717—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Undecynyl)benzaldehydeHCID 1837309113.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 3-bromobenzaldehyde (51.8 g), 1-undecyne (48.6 g), bis(triphenylphosphine)palladium(II)chloride (3.37 g), copper iodide (457 mg), and triethylamine (196 ml) in dry tetrahydrofuran (300 ml) was stirred for 4 hrs at 55° C. The reaction mixture was filtered, the filtrate was diluted with ethyl acetate, and the solution was washed with water and brine. The organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on 300 g of silica gel (1:4-ethyl acetate:hexane). The appropriate fractions were collected and evaporated. Distillation of a 40-g sample of the residue (81.3 g) gave 9.5 g (13%) of the product, bp 172°-174° C. (0.5 mm mercury).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534640
Source datasetuspto-grants-1996_07
ORD IDord-92cf7bb393e24af39cef518c55c55a3c
Source noteuspto-grants-1996_07