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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61417생성일: 2026년 10월 25일

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(4-cyano-2-methylphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/61417

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물4-Bromo-3-methylbenzonitrileHCID 2737494—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(4-cyano-2-methylphenyl)piperazine-1-carboxylateHCID 6005111186.9%

반응 단계

To a nitrogen flushed flask containing PdCl2dppf (65.8 mg, 0.081 mmol), dppf (44.6 mg, 0.081 mmol) and 4-bromo-3-methylbenzonitrile (631 mg, 3.22 mmol) in THF (5 mL) at −78° C. was added tert-butyl 1-piperazinecarboxylate (500 mg, 2.68 mmol) as a solid. The resultant mixture was heated to 100° C. and vigorously stirred overnight under nitrogen. The reaction was quenched with water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash chromatography (eluting with 0 to 30% ethyl acetate in hexane) to afford 4-(4-cyano-2-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (702 mg, 86.9%). MS (ESI): 302.0 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440958B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-0cc5f5dc19fe4cd4a5877ca158cdb183
출처 메모uspto-grants-2016_09