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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458306Generated: October 27, 2026

4-(4-Fluoro-3-methylphenyl)-4-oxobutanoic acid → 4-(4-Fluoro-3-methylphenyl)butanoic acid

https://huagongshe.com/reaction/1458306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Fluoro-3-methylphenyl)-4-oxobutanoic acidHCID 6485443—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product4-(4-Fluoro-3-methylphenyl)butanoic acidHCID 649707287.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a 50-ml autoclave, 1.0 g of 4-(4-fluoro-3 -methylphenyl)-4-oxobutanoic acid and 2.5 ml of methanol were charged, followed by the addition of 0.1 g of 10% palladium-carbon. After hydrogen pressure was increased to 30 kg/cm2 at room temperature, the resulting mixture was stirred at 50° C. for 3.5 hours. After the completion of the reaction, the reaction mixture was filtered, followed by washing with methanol. The filtrate was thereafter concentrated under reduced pressure. Water was added to the residue so obtained. The crystals so precipitated were filtered, washed with water and dried under reduced pressure, whereby 0.82 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849945
Source datasetuspto-grants-1998_12
ORD IDord-fb4f002e781a478cbe1ffd35a52ac052
Source noteuspto-grants-1998_12