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HRID 243生成日期:2026年10月23日

4-溴苯酚 → 4-(4-Methyl-1-piperazinyl)phenol

https://huagongshe.com/zh-CN/reaction/243

反应方程式

参与物

角色名称HCID投料
反应物4-溴苯酚HCID 7808—
反应物N-甲基哌嗪HCID 53167—
试剂双三甲基硅基胺基锂HCID 2733832—
催化剂醋酸钯HCID 4144353—
催化剂2,8,9-三异丁基-2,5,8,9-四氮杂-1-磷酸双向环[3.3.3]十一烷HCID 4571243—
溶剂甲苯HCID 1140—
产物4-(4-Methyl-1-piperazinyl)phenolHCID 1162248650.99%

反应条件

温度80 °C

反应步骤

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.

来源与证据

来源数据集750 AstraZeneca ELN dataset
ORD IDord-8e16338c39aa405d9e6607bfaa8d820e
来源说明750 AstraZeneca ELN dataset