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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950005Generated: October 27, 2026

Triethylamine → 1-[3-(4-Bromo-2-fluorophenyl)prop-2-ynyl]piperidine

https://huagongshe.com/reaction/1950005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Prop-2-yn-1-yl)piperidineHCID 336652—
Reactant4-Bromo-2-fluoro-1-iodobenzeneHCID 2724516—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product1-[3-(4-Bromo-2-fluorophenyl)prop-2-ynyl]piperidineHCID 2308756544.7%

Reaction Steps

To a solution of 1-bromo-3-fluoro-4-iodobenzene (2.5 g), 1-prop-2-ynylpiperidine (1.5 g), dichlorobis(triphenylphosphine)palladium(II) (300 mg) and copper(I) iodide (40 mg) in N,N-dimethylformamide (20 ml) was added triethylamine (10 ml) under a nitrogen atmosphere, and the solution was stirred for 1.5 hours at room temperature. A saturated aqueous solution of ammonium chloride was added thereto followed by stirring, the solution was extracted with ethyl acetate, then sequentially washed with water and brine, and dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (1.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399520B2
Source datasetuspto-grants-2013_03
ORD IDord-f9ee1b45113448f7b2b03cc765f6d959
Source noteuspto-grants-2013_03