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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1863538생성일: 2026년 10월 27일

Water → 3-Hydroxy-3-phenylbutan-2-one

https://huagongshe.com/reaction/1863538

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sulfuric AcidHCID 1118—
반응물3-Hydroxy-3-phenyl-1-butyneHCID 92098—
용매MethanolHCID 887—
생성물3-Hydroxy-3-phenylbutan-2-oneHCID 233220—

반응 조건

온도55 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04169202
출처 데이터셋uspto-grants-1979_09
ORD IDord-7da86fbf0431441790e160a8a351bd48
출처 메모uspto-grants-1979_09