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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 332655생성일: 2026년 10월 25일

Triphenylphosphine → (3-(4-((1,3-Dioxolan-2-yl)methyl)benzyloxy)phenyl)-(phenyl)methanone

https://huagongshe.com/reaction/332655

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-HydroxybenzophenoneHCID 83050—
반응물(4-((1,3-Dioxolan-2-yl)methyl)phenyl)methanolHCID 86676898—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(3-(4-((1,3-Dioxolan-2-yl)methyl)benzyloxy)phenyl)-(phenyl)methanoneHCID 71113108117.8%

반응 단계

To a cooled (0° C.) solution of (4-((1,3-dioxolan-2-yl)methyl)phenyl)methanol (0.45 g, 2.317 mmol), 3-hydroxybenzophenone (0.551 g, 2.78 mmol) and triphenylphosphine (0.729 g, 2.78 mmol) in anhydrous THF, di-iso-propylazodicarboxylate (1.027 mL, 2.78 mmol) was added dropwise. The reaction mixture was allowed to warm to RT and stirred at this temperature for 16 hours. The reaction mixture was diluted with ethyl acetate and washed with 10% aqueous potassium carbonate, brine and dried (magnesium sulfate). The suspension was filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 100% iso-hexane to 25% ethyl acetate in iso-hexane to afford the title compound (1.022 g, >100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877774B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-25d0f516749b4f2e97a0a4f49ecfd867
출처 메모uspto-grants-2014_11