Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743783Generated: October 30, 2026

Triethylamine → HCID 18372930, compound

https://huagongshe.com/reaction/743783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 561991HCID 561991—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18372930HCID 1837293068.4%

Reaction Steps

A solution of 6-bromopyridine-2-carboxaldehyde (30.0 g), 7-phenyl-1-heptyne (26.8 g), triethylamine (48.9 g), bis(triphenylphosphine)palladium(II)chloride (2.3 g, 2%), and copper(I)iodide (0.31 g, 1%) in dry tetrahydrofuran (100 ml) was heated under nitrogen at 55° C. for 70 hrs. The reaction mixture was cooled to ambient temperature, filtered, and the filtrate was washed with ethyl acetate. The filtrate was evaporated. The residue was dissolved in ethyl acetate, the solution washed with half-saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the filtrate was concentrated. The residue was flash chromatographed on silica gel, eluting with 0.5% to 2%-ethyl acetate:hexane. The appropriate fractions were collected and concentrated to yield 29.5 g of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05557006
Source datasetuspto-grants-1996_09
ORD IDord-dec35a6bc47542d5b5e79b76e8f434b0
Source noteuspto-grants-1996_09