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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863538Generated: October 26, 2026

Water → 3-Hydroxy-3-phenylbutan-2-one

https://huagongshe.com/reaction/1863538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
Reactant3-Hydroxy-3-phenyl-1-butyneHCID 92098—
SolventMethanolHCID 887—
Product3-Hydroxy-3-phenylbutan-2-oneHCID 233220—

Reaction Conditions

Temperature55 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04169202
Source datasetuspto-grants-1979_09
ORD IDord-7da86fbf0431441790e160a8a351bd48
Source noteuspto-grants-1979_09