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HRID 474249作成日:2026年10月24日

Formic Acid → 2-Phenylcyclopentanone

https://huagongshe.com/ja/reaction/474249

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物Hydrogen PeroxideHCID 784—
反応物Benzene, 1-cyclopenten-1-yl-HCID 136652—
生成物2-PhenylcyclopentanoneHCID 29015484%

反応条件

温度40 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637523B2
出典データセットuspto-grants-2014_01
ORD IDord-9a9917518e824512ab20c9750debc3b7
出典メモuspto-grants-2014_01