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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280생성일: 2026년 10월 23일

7-Bromo-1-benzofuran → Tert-butyl 4-(7-benzo[b]furanyl)piperazine-1-carboxylate

https://huagongshe.com/ko/reaction/280

반응식

참여 물질

역할이름HCID투입량
반응물7-Bromo-1-benzofuranHCID 113628—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
시약Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(7-benzo[b]furanyl)piperazine-1-carboxylateHCID 2330001284.06%

반응 조건

온도100 °C

반응 단계

7-bromobenzofuran (2 g, 10.15 mmol), tert-Butyl 1-piperazinecarboxylate (1.891 g, 10.15 mmol), Tris(dibenzylideneacetone)dipalladium(0) (0.465 g, 0.51 mmol), 2-Dicyclohexylphosphino-2',4',6'-tri-iso-propyl-1,1'-biphenyl (0.484 g, 1.02 mmol) and sodium t-butoxide (1.856 mL, 21.32 mmol) were heated to 100 °C in toluene (10 mL) for 3h. The mixture was allowed to cool to ambient temperature. Ethylacetate was added and the mixture was filtered through Celite. The filtrate was concentrated and redissolved in ethylacetate. The organic mixture was washed with satd. aqueous Na2CO3 and brine. The organic phase was separated, dried over Na2CO3, filtered and the solvent removed by rotary evaporation. The crude product was redissolved in diethylether and loaded onto a silica gel column and eluted with 0-50% EtOAc in heptanes. The collected fractions were combined and the solvent removed by rotary evaporation to yield tert-butyl 4-(benzofuran-7-yl)piperazine-1-carboxylate (2.58 g, 84 %). MS (m+1) = 303. HPLC Peak RT = 5.97 minutes is product. Purity = 94%.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-decd3260950345c1bc7b269e3329c8ac
출처 메모750 AstraZeneca ELN dataset