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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545325Generated: October 29, 2026

1-Hexyne → HCID 11424006, compound

https://huagongshe.com/reaction/545325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HexyneHCID 12732—
Reactant3-BromobenzaldehydeHCID 76583—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventPiperidineHCID 8082—
ProductHCID 11424006HCID 1142400687.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 10.0 g (54.05 mmol) of 3-bromo-benzaldehyde in 150 ml of piperidine was treated at RT with 1.029 g (5.40 mmol) of copper(I)iodide and 6.246 g (5.40 mmol) of tetrakis-(triphenylphosphine)-palladium and the mixture was then warmed up to 60° C. After 10 min, a solution of 9.30 ml=6.66 g (81.07 mmol) of hex-1-yne in 150 ml of piperidine was added drop by drop during 1 hour. After 30 min, the oil bath temperature was steadily increased to 80° C. The reaction mixture was then stirred at 80° C. for 15 hours and subsequently cooled down to RT. The solvent was evaporated and the residue poured into crashed ice, acidified with HCl (37%) to pH 2-3 and extracted twice with EtOAc; the organic phases were washed with water, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography (n-heptane/EtOAc 1:0 to 97:3) to give 8.78 g (87%) of the title compound as yellow oil. MS: 186.2 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935707B2
Source datasetuspto-grants-2011_05
ORD IDord-967e1a0031f040539f4e96651194cf6c
Source noteuspto-grants-2011_05