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HRID 343作成日:2026年10月23日

1-Bromo-4-fluorobenzene → 1-Benzyl-4-(4-fluorophenyl)piperazine

https://huagongshe.com/ja/reaction/343

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-4-fluorobenzeneHCID 9993—
反応物1-BenzylpiperazineHCID 75994—
試薬Sodium t-butoxideHCID 23676156—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Palladium (II) acetateHCID 4144353—
溶媒TolueneHCID 1140—
生成物1-Benzyl-4-(4-fluorophenyl)piperazineHCID 76319974.98%

反応条件

温度50 °C

反応手順

diacetoxypalladium (12.74 mg, 0.06 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (32.8 mg, 0.06 mmol) were suspended in toluene (0.5 mL) under N2. Heated to 50C for 30 min (microwave). sodium 2-methylpropan-2-olate (109 mg, 1.13 mmol) was suspended in toluene (0.500 mL) under N2. 1-benzylpiperazine (0.099 mL, 0.57 mmol) and 1-bromo-4-fluorobenzene (0.093 mL, 0.85 mmol) were added, followed by the catalyst solution. Heated to 100C for 2h in the microwave (high abs), then rt over night. The product was purified on silica (0-25% EtOAc/heptane) Yield: 1-benzyl-4-(4-fluorophenyl)piperazine (115 mg, 75.0 %)

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-8809d217cb404d41bb5809dd5f95b269
出典メモ750 AstraZeneca ELN dataset