Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 243Erstellt: 23. Oktober 2026

4-Bromophenol → 4-(4-Methyl-1-piperazinyl)phenol

https://huagongshe.com/de/reaction/243

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromophenolHCID 7808—
Edukt1-MethylpiperazineHCID 53167—
ReagenzLithium HexamethyldisilazideHCID 2733832—
KatalysatorPalladium (II) acetateHCID 4144353—
Katalysator2,8,9-Triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecaneHCID 4571243—
LösungsmittelTolueneHCID 1140—
Produkt4-(4-Methyl-1-piperazinyl)phenolHCID 1162248650,99%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

diacetoxypalladium (0.039 g, 0.17 mmol) was added in one portion to 4-bromophenol (3 g, 17.34 mmol) and 1-methylpiperazine (2.308 mL, 20.81 mmol) in toluene (87 mL) at 25°C under nitrogen. To this was added toluene (87 mL) then a solution of 2,8,9-triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane (0.123 mL, 0.35 mmol) in Toluene (1 mL) and finally 1M LITHIUM BIS(TRIMETHYLSILYL)AMIDE (39.9 mL, 39.88 mmol) in THF was added dropwise over 1 minute. The resulting mixture was stirred at 80 °C for 18 hours. The reaction was allowed to cool to room temperature, SiO2 (23g) was added and evaporated to dryness. The crude product was purified by flash silica chromatography (120g), elution gradient 0 to 10% MeOH in EtOAc. Pure fractions were evaporated to dryness to afford 4-(4-methylpiperazin-1-yl)phenol (1.700 g, 51.0 %) as a beige solid.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-8e16338c39aa405d9e6607bfaa8d820e
Quellennotiz750 AstraZeneca ELN dataset