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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030868Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1030868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromopentafluorobenzeneHCID 9578—
EduktBenzenamine, 3-ethynyl-HCID 104682—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorBis(triphenylphosphine)palladiumHCID 10122028—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-[(2,3,4,5,6-Pentafluorophenyl)ethynyl]anilineHCID 1982108250%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05107026
Quelldatensatzuspto-grants-1992_04
ORD IDord-8f5f3815000a48febbaff23a56453646
Quellennotizuspto-grants-1992_04