Ethanol → 1-Cycloperityl-3-(4-phenoxyphenyl)propane-1,3-dione

HRID 81011

반응식

HRID 81011 반응식
[H-].[Na+].[CH:3]1([C:8]([O:10]C)=O)[CH2:7][CH2:6][CH2:5][CH2:4]1.[O:12]([C:19]1[CH:24]=[CH:23][C:22]([C:25](=[O:27])[CH3:26])=[CH:21][CH:20]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(O)C>C1COCC1>[CH:3]1([C:8](=[O:10])[CH2:26][C:25]([C:22]2[CH:23]=[CH:24][C:19]([O:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:20][CH:21]=2)=[O:27])[CH2:4][CH2:5][CH2:6][CH2:7]1

참가 물질

6

실험 절차

Sodium hydride (1.508 g, 37.7 mmol, 60% suspension in mineral oil) was added in small portions to a solution of methyl cyclopentanecarboxylate (1.449 g, 11.31 mmol) and 1-(4-phenoxyphenyl)ethanone (2.00 g, 9.42 mmol) in THF (100 mL). Ethanol (0.5 mL) was then added. The mixture was heated to reflux for 5.5 h, quenched with saturated NaCl (50 mL) and acidified to pH 2 with 1 N HCl. THF was evaporated in vacuo. The residue was extracted with ethyl acetate (3×50 mL). The combined extracts were washed with brine (10 mL), dried (MgSO4) and concentrated. Silica gel chromatography, loading with 5% ethyl acetate in hexanes and eluting with 5-20% ethyl acetate in hexanes, gave 1-cycloperityl-3-(4-phenoxyphenyl)propane-1,3-dione as white solid (1.837 g, 63% yield). MS (ES+) m/z: 309 (M+H); LC retention time: 5.015 min (analytical HPLC Method A).

후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 5.5 h
  3. customquenched with saturated NaCl (50 mL)
  4. customTHF was evaporated in vacuo
  5. extractionThe residue was extracted with ethyl acetate (3×50 mL)
  6. washThe combined extracts were washed with brine (10 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated
  9. washeluting with 5-20% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-07bdb1babcf84960ac0c28d5d4cad1b1
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08846673B2

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