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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389555Generated: October 25, 2026

Water → 3-Hydroxy-3-phenylbutan-2-one

https://huagongshe.com/reaction/1389555

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 0.5 g of the title compound, ir(CHCl3)3450 and 1751 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 numberUS04244958
Source datasetuspto-grants-1981_01
ORD IDord-9234af1330c640c194494c41b493b12c
Source noteuspto-grants-1981_01