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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1515492생성일: 2026년 10월 26일

1-Bromo-4-iodobenzene → 4-Benzyl-1-(4-bromophenyl)piperidine

https://huagongshe.com/reaction/1515492

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-4-iodobenzeneHCID 11522—
반응물1,1'-BinaphthylHCID 11789—
반응물4-BenzylpiperidineHCID 31738—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TetrahydrofuranHCID 8028—
생성물4-Benzyl-1-(4-bromophenyl)piperidineHCID 12169538—

반응 단계

A mixture of 1-bromo-4-iodo benzene (0.500 g), 4-benzylpiperidine (0.25 mL), sodium-tert-butylate (0.238 g), tris(dibenzylideneacetone)dipalladium (0.016 g) and 2,2′-bis/diphenylphosphino)-1,1′-binaphtyl racemate (0.018 g) is dissolved in tetrahydrofuran and stirred at room temperature overnight. The reaction mixture is concentrated and the resulting residue is loaded on Celite and purified by silica gel chromatography (4:1 hexanes/ethyl acetate) to give 4-benzyl-1-(4-bromo-phenyl)-piperidine as a light yellow syrup. MS (m/z): 331 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08222424B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-c7e2ef58bbbd47189b8620af00d349ed
출처 메모uspto-grants-2012_07