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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 281생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/281

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 2330001272.98%

반응 조건

온도100 °C

반응 단계

7-bromobenzofuran (500 mg, 2.54 mmol), tert-Butyl 1-piperazinecarboxylate (473 mg, 2.54 mmol), Tris(dibenzylideneacetone)dipalladium(0) (116 mg, 0.13 mmol), 2-Dicyclohexylphosphino-2',4',6'-tri-iso-propyl-1,1'-biphenyl (121 mg, 0.25 mmol) and sodium t-butoxide (0.464 mL, 5.33 mmol) were heated in toluene (2 mL) to 100 °C for 2h. The mixture was allowed to cool. 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 added to a silica gel column and was eluted with 0-2% MeOH in DCM and to a second silica gel column eluted with 0-100% EtOAc in heptane. The collected fractions were combined to yield tert-butyl 4-(benzofuran-7-yl)piperazine-1-carboxylate (560 mg, 73.0 %). 1H NMR in CD3OD is consistent with desired product MS (m+1) = 303.1. HPLC Peak RT = 5.99 minutes is product. Purity = 98%.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-bfb17eeff42440ec958bdd65e83b7c45
출처 메모750 AstraZeneca ELN dataset