돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 630생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Benzonitrile, 4-bromo-HCID 12162—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylateHCID 279551282.34%

반응 조건

온도120 °C

반응 단계

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

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-587e8b015ef542aa9ba95a064a0d6902
출처 메모750 AstraZeneca ELN dataset