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HRID 42201Erstellt: 23. Oktober 2026

Benzene, 1-bromo-4-(trifluoromethyl)- → HCID 25065679, Verbindung

https://huagongshe.com/de/reaction/42201

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
Edukt1-Benzyl-4-piperazin-1-yl-phthalazineHCID 6404023—
Edukt2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
EduktPotassium tert-butoxideHCID 23665647—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 25065679HCID 2506567937%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

To a solution of 1-benzyl-4-piperazin-1yl-phthalazine (100 mg, 0.329 mmol) in 1 mL THF is added 4-bromo-benzotrifluoride (99 mg, 0.443 mmol), potassium tert-butoxide (55.3 mg, 0.493 mmol), XPhos [2-(Dicyclohexylphosphino)-2′,4′,6′-tri-1-propyl-1′-1′-biphenyl] (15.7 mg, 0.033 mmol), and palladium (II) acetate (11 mg, 0.16 mmol) in a 2 dram screw-top vial. The vial is evacuated and flushed with argon. The reaction mixture was heated to 110° C. for 18 hrs. The mixture is then poured into water (50 mL), and the precipitate is isolated by filtration. The resulting solid is purified by flash chromatography on silica gel (10-70% EtOAc:heptanes) to provide the desired product as yellow crystals (54 mg, 37% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536168B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-a0263b0c12aa448d90f3cddfd3abef19
Quellennotizuspto-grants-2013_09