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HRID 243作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromophenolHCID 7808—
反応物1-MethylpiperazineHCID 53167—
試薬Lithium HexamethyldisilazideHCID 2733832—
触媒Palladium (II) acetateHCID 4144353—
触媒2,8,9-Triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecaneHCID 4571243—
溶媒TolueneHCID 1140—
生成物4-(4-Methyl-1-piperazinyl)phenolHCID 1162248650.99%

反応条件

温度80 °C

反応手順

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.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-8e16338c39aa405d9e6607bfaa8d820e
出典メモ750 AstraZeneca ELN dataset