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HRID 630作成日:2026年10月23日

Benzonitrile, 4-bromo- → Tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylate

https://huagongshe.com/ja/reaction/630

反応式

関与物質

役割名称HCID仕込み量
反応物Benzonitrile, 4-bromo-HCID 12162—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
試薬Sodium t-butoxideHCID 23676156—
触媒Palladium (II) acetateHCID 4144353—
触媒2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylateHCID 279551282.34%

反応条件

温度120 °C

反応手順

To 4-bromobenzonitrile (.5 g, 2.75 mmol) dissolved in dry THF (10 mL) was added tert-butyl piperazine-1-carboxylate (0.512 g, 2.75 mmol), Sodium-t- butoxide (0.792 g, 8.24 mmol) and purged with N2 gas for 10 min followed by the addition of 2-(Dicyclohexylphosphino)-2',4',6'-tri-i-propyl-1,1'-biphenyl (0.131 g, 0.27 mmol)and Palladium II acetate (0.062 g, 0.27 mmol). The contents were further purged with N2 gas for further 10 min and heated at 85 °C for 2 h. The reaction mass was concentrated and the reside diluted with water and extracted with ethyl acetate . The combined organic extracts were washed with brine solution and dried over anhydrous sodium sulphate. The organic layer was evaporated under reduced pressure to obtain the crude product which was purified by 60-120 mesh silica gel column chromatography using 25% Ethyl acetate : Hexanes mixture to obtain tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylate (0.650 g, 82 %) as a white solid. m/z (ES+), M+ = 288.4

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-587e8b015ef542aa9ba95a064a0d6902
出典メモ750 AstraZeneca ELN dataset