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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343Erstellt: 23. Oktober 2026

1-Bromo-4-fluorobenzene → 1-Benzyl-4-(4-fluorophenyl)piperazine

https://huagongshe.com/de/reaction/343

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-4-fluorobenzeneHCID 9993—
Edukt1-BenzylpiperazineHCID 75994—
ReagenzSodium t-butoxideHCID 23676156—
Katalysator1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
KatalysatorPalladium (II) acetateHCID 4144353—
LösungsmittelTolueneHCID 1140—
Produkt1-Benzyl-4-(4-fluorophenyl)piperazineHCID 76319974,98%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

diacetoxypalladium (12.74 mg, 0.06 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (32.8 mg, 0.06 mmol) were suspended in toluene (0.5 mL) under N2. Heated to 50C for 30 min (microwave). sodium 2-methylpropan-2-olate (109 mg, 1.13 mmol) was suspended in toluene (0.500 mL) under N2. 1-benzylpiperazine (0.099 mL, 0.57 mmol) and 1-bromo-4-fluorobenzene (0.093 mL, 0.85 mmol) were added, followed by the catalyst solution. Heated to 100C for 2h in the microwave (high abs), then rt over night. The product was purified on silica (0-25% EtOAc/heptane) Yield: 1-benzyl-4-(4-fluorophenyl)piperazine (115 mg, 75.0 %)

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-8809d217cb404d41bb5809dd5f95b269
Quellennotiz750 AstraZeneca ELN dataset