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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356455생성일: 2026년 10월 25일

3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-one → 3-(4-Benzyloxy-phenyl)-1-cyclohexyl-propan-1-one

https://huagongshe.com/reaction/356455

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-oneHCID 471477—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물3-(4-Benzyloxy-phenyl)-1-cyclohexyl-propan-1-oneHCID 18798668—

반응 단계

The title compound was prepared by hydrogenation of 3-(4-benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-one (25.85 g, 84 mmol; prepared in Example C) as described in General Method 3 using 1.0 g of 5% Pd on BaSO4 in 600 mL of THF at room temperature. The crude product was flash chromatographed using CH2Cl2 :MeOH (99:1 to 98:2) to afford a gummy solid. 1H NMR (CDCl3) δ 1.1-1.9 (m, 10 H), 2.2-2.4 (m, 1 H), 2.68-2.74 (m, 2 H), 2.79-2.85 (m, 2 H), 5.04 (s, 2 H), 6.8-6.9 (d, 2 H), 7.1-7.2 (d, 2 H), 7.3-7.5 (m, 5 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834506
출처 데이터셋uspto-grants-1998_11
ORD IDord-b8cad75ea5614c819a8cdbdfd65e0b73
출처 메모uspto-grants-1998_11