Reaktion #339

ord-8e16338c39aa405d9e6607bfaa8d820e

Reaktionsgleichung

Oc1ccc(Br)cc1
Oc1ccc(Br)cc1
CN1CCNCC1
CN1CCNCC1
CN1CCN(c2ccc(O)cc2)CC1
CN1CCN(c2ccc(O)cc2)C
Ausbeute 51.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS

Vorschrift

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.

Quelle

750 AstraZeneca ELN dataset