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HRID 1863538作成日:2026年10月27日

Water → 3-Hydroxy-3-phenylbutan-2-one

https://huagongshe.com/reaction/1863538

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sulfuric AcidHCID 1118—
反応物3-Hydroxy-3-phenyl-1-butyneHCID 92098—
溶媒MethanolHCID 887—
生成物3-Hydroxy-3-phenylbutan-2-oneHCID 233220—

反応条件

温度55 °C

反応手順

The title compound is prepared by using a modified method of G. F. Hennion and B. R. Fleck, J. Amer. Chem. Soc., 77,3258(1955). To a mixture of methanol (5 ml), water (0.2 ml), sulfuric acid (100 mg), and mercuric sulfate (100 mg) is added at 55° C. a solution of 3-hydroxy-3-phenyl-1-butyne (2 g) in 90% aqueous methanol (5 ml) over a period of 90 min. The reaction is slightly exothermic, and the inside temperature is maintained at 55°-57° C. During the reaction time, 50 mg of mercuric sulfate is added. When addition of the acetylenic component is complete, another portion (50 mg) of mercuric sulfate is added, and the mixture is stirred at 55° C. for 1 hour. During this time 1 ml of water is added. After cooling, the reaction mixture is poured into ice-water and extracted with diethyl ether. The combined extracts are washed with water, dried over magnesium sulfate, filtered and evaporated. The resultant oil is chromatographed on silica gel using benzene. The appropriate eluates are evaporated to give 0.5g of the title compound, ir(CHCl3)3450 and 1741 cm-1 and nmr(CDCl3) δ 1.75(s), 2.08(s), 4.50(s) and 7.40(m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04169202
出典データセットuspto-grants-1979_09
ORD IDord-7da86fbf0431441790e160a8a351bd48
出典メモuspto-grants-1979_09