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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030868Generated: October 25, 2026

Bromopentafluorobenzene → 3-[(2,3,4,5,6-Pentafluorophenyl)ethynyl]aniline

https://huagongshe.com/reaction/1030868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromopentafluorobenzeneHCID 9578—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
CatalystTriphenylphosphineHCID 11776—
CatalystBis(triphenylphosphine)palladiumHCID 10122028—
SolventDiethyl EtherHCID 3283—
Product3-[(2,3,4,5,6-Pentafluorophenyl)ethynyl]anilineHCID 1982108250%

Reaction Conditions

Temperature70 °C

Reaction Steps

A multinecked flash as described in Example 1 was charged with 5.0 g (0.020 mol) of bromopentafluoro-benzene, 2.37 g (0.020 mol) of 3-aminophenylacetylene, 0.096 g (0.137 mmol) of bis(triphenylphosphine) palladium II chloride, 0.148 g (0.564 mmol) of triphenylphosphine, and 0.06 g (0.315 mmol) of cuprous iodide. The reaction mixture was heated at 70° C. for 40 hours after which gas chromatography showed the reaction to be complete. The product mixture was cooled to room temperature and diluted with 75 ml of ether. Filtration of the insoluble triethylamine hydrobromide salt by-product followed by concentration of the filtrate gave 5.7 g, (0.02 mol) of crude product as a yellow solid. Short path distillation of the crude under reduced pressure gave 2.84 g (0.010 mol, 50% yield) of the product as a colorless liquid that crystallized on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05107026
Source datasetuspto-grants-1992_04
ORD IDord-8f5f3815000a48febbaff23a56453646
Source noteuspto-grants-1992_04