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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-BromophenolHCID 7808—
반응물1-MethylpiperazineHCID 53167—
시약Lithium HexamethyldisilazideHCID 2733832—
촉매Palladium (II) acetateHCID 4144353—
촉매2,8,9-Triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo(3.3.3)undecaneHCID 4571243—
용매TolueneHCID 1140—
생성물4-(4-Methyl-1-piperazinyl)phenolHCID 1162248650.99%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-8e16338c39aa405d9e6607bfaa8d820e
출처 메모750 AstraZeneca ELN dataset