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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 553028생성일: 2026년 10월 26일

Triphenylphosphine → 2-[(3S)-1-azabicyclo[2.2.2]octan-3-yloxy]-fluoren-9-one

https://huagongshe.com/reaction/553028

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2-Hydroxyfluoren-9-oneHCID 81386—
반응물3-Quinuclidinol, (-)-HCID 91404—
반응물Diethyl azodicarboxylateHCID 5462977—
용매TetrahydrofuranHCID 8028—
생성물2-[(3S)-1-azabicyclo[2.2.2]octan-3-yloxy]-fluoren-9-oneHCID 1122046634%

반응 단계

To a 0° C. mixture of 2-hydroxyfluoren-9-one (196 mg, 1.00 mmol; Aldrich), (3R)-quinuclidin-3-ol (151 mg, 1.20 mmol; Acros), and polymer-bound triphenylphosphine (500 mg, 3 mmol/g; Aldrich) in THF (5 mL) was added diethylazodicarboxylate (200 μL, 1.27 mmol; Aldrich). After 1 h, the reaction mixture was allowed to warm to room temperature and was stirred overnight (16 h). The mixture was filtered through diatomaceous earth, the filter pad rinsed with dichloromethane, and the organic extracts purified twice by flash chromatography (80 g silica gel, eluting with 1-5% of 10% NH4OH/MeOH in CH2Cl2) to afford the title compound (104 mg, 0.340 mmol, 34% yield). MS (DCI/NH3): m/z 306 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951791B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-a417337957c34d5e9aa7f3755d9eb191
출처 메모uspto-grants-2011_05