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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(4-Fluoro-3-methylphenyl)-4-oxobutanoic acid | HCID 6485443 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-Fluoro-3-methylphenyl)butanoic acid | HCID 6497072 | 87.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849945 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-fb4f002e781a478cbe1ffd35a52ac052 |
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| Source note | uspto-grants-1998_12 |
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