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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1166534생성일: 2026년 10월 26일

Sodium Chloride → 6-(3'-Aminobiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin hydrochloride

https://huagongshe.com/reaction/1166534

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium CarbonateHCID 10340—
반응물6-(4-bromobenzyl)oxy-2-[2-(N,N-dimethylamino)ethyl]tetralinHCID 18361484—
반응물3-Aminophenylboric acidHCID 21895836—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물6-(3'-Aminobiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin hydrochlorideHCID 18361523—

반응 단계

An ethanol solution (10 ml) of 3-aminophenylboric acid (1.3 g) and an aqueous 2M sodium carbonate solution (10 ml) were added to a toluene solution (80 ml) of 6-(4-bromobenzyl)oxy-2-[2-(N,N-dimethylamino) ethyl]tetralin (3.00 g) and tetrakis-(triphenylphosphine) palladium (0.45 g). The reaction mixture was heated under reflux for 12 hours in an argon atmosphere. A saturated aqueous sodium chloride solution was added to this, which was then extracted with ethyl acetate. The organic layer was dried, and then concentrated. The residue was purified by alumina column chromatography (eluent: ethyl acetate/hexane=1/2), and then processed with 4 N hydrochloric acid-ethyl acetate to form a hydrochloride. The thus-formed salt was recrystallized from methanol-diisopropyl ether to obtain the entitled compound (0.78 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06613805B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-03c15fedcc0548d2ab238ed924c81311
출처 메모uspto-grants-2003_09