反応式
OO.[CH:3]([OH:5])=O.[C:6]1([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)C[CH2:9][CH2:8][CH:7]=1>>[C:11]1([CH:6]2[CH2:7][CH2:8][CH2:9][C:3]2=[O:5])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1参加物
反応条件
- 温度
- 40 °C
実験手順
A mixture of 30% hydrogen peroxide (23 mL, 149 mmol) and 85% formic acid (100 mL, 2619 mmol) was heated at 40° C. for 15 min. The mixture was carefully added to cyclopentenylbenzene (21.49 g, 149 mmol) and the resulting two-phase system was vigorously stirred at room temperature for 4 h. An exothermic reaction was observed in the beginning. By the end of the stirring the solution had become homogeneous. The reaction mixture was carefully quenched with a saturated aqueous solution of sodium bicarbonate. The product was extracted with ether. The combined etherial layers were dried over anhydrous magnesium sulfate and filtered. The solvent was removed in vacuo and the product was purified by column chromatography on silica gel to give 2-phenylcyclopentanone (19.995 g, 125 mmol, 84% yield) as a brown oil. LC-MS (M+H)+=161.0. 1H NMR (500 MHz, chloroform-d) δ ppm 7.38 (1H, t, J=7.3 Hz), 7.30-7.35 (2H, m), 7.19 (2H, d, J=7.3 Hz), 3.28-3.37 (1H, m), 2.71 (1H, td, J=4.6, 2.7 Hz), 2.58-2.63 (1H, m), 2.43-2.55 (1H, m), 2.29 (1H, ddd, J=19.0, 10.5, 9.0 Hz), 2.07-2.21 (1H, m), 1.88-1.99 (1H, m).
後処理
- customAn exothermic reaction
- customThe reaction mixture was carefully quenched with a saturated aqueous solution of sodium bicarbonate
- extractionThe product was extracted with ether
- dry with materialThe combined etherial layers were dried over anhydrous magnesium sulfate
- filtrationfiltered
- customThe solvent was removed in vacuo
- customthe product was purified by column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-9a9917518e824512ab20c9750debc3b7
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637523B2
関連ノート
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