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

HRID 243

Reaktionsgleichung

Reaktionsgleichung von HRID 243
CN1CCNCC1.Oc1ccc(Br)cc1>CC(=O)O.CC(=O)O.CC(C)CN1CCN2CCN(CC(C)C)P1N(CC(C)C)CC2.C[Si](C)(C)[N-][Si](C)(C)C.Cc1ccccc1.[Li+].[Pd]>CN1CCN(c2ccc(O)cc2)CC1

Komponenten

7

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

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.

Quellen und Nachweise

ORD-Eintrag
ord-8e16338c39aa405d9e6607bfaa8d820e
Quelldatensatz
750 AstraZeneca ELN dataset
Originallink
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