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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568072Generated: November 1, 2026

Sodium Hydroxide → HCID 15383979, compound

https://huagongshe.com/reaction/568072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 54386099HCID 54386099—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 15383979HCID 1538397915.5%

Reaction Steps

3.3 g of sodium hydroxide dissolved in 10 ml of water are added to a solution of 29.3 g of ethyl 3-(3-fluorophenyl)-3-(4-methanesulphonylphenyl)-2-(2-hydroxyethyl)-2-propenoate, prepared in Example 12, in 50 ml of ethanol and the mixture is refluxed for 2 hours. After evaporation to dryness, the residue is taken up with water, acidified with 1 N hydrochloric acid and then extracted with dichloromethane. The organic phase is dried over magnesium sulphate and evaporated under vacuum to give an oily residue. The oil is solubilized in 150 ml of toluene, and 10 mg of paratoluenesulphonic acid are added. The mixture is refluxed and the water formed is removed with a Dean-Stark apparatus. After cooling, the mixture is washed with water, the organic phase is dried over magnesium sulphate and evaporated under vacuum and the residue is chromatographed on silica in t-butyl methyl ether to give 4 g of (Z)-3-[1-(3-fluorophenyl)-1-(4-methanesulphonylphenyl)methylidene]dihydrofuran-2-one (2nd product eluted) in the form of crystals melting at 153-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180651B2
Source datasetuspto-grants-2001_01
ORD IDord-6d0527fb590e481285e34d04b6e41802
Source noteuspto-grants-2001_01