Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-one → 3-(4-Benzyloxy-phenyl)-1-cyclohexyl-propan-1-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-(4-Benzyloxy-phenyl)-1-cyclohexyl-prop-2-en-1-one | HCID 471477 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(4-Benzyloxy-phenyl)-1-cyclohexyl-propan-1-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05834506 |
| 출처 데이터셋 | uspto-grants-1998_11 |
| ORD ID | ord-b8cad75ea5614c819a8cdbdfd65e0b73 |
| 출처 메모 | uspto-grants-1998_11 |