HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731164Generated: November 2, 2026
4-(2-Methyl-3-(4-chlorobenzoyl)phenyl)butanoic acid → HCID 21495671, compound
https://huagongshe.com/reaction/1731164
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(2-Methyl-3-(4-chlorobenzoyl)phenyl)butanoic acid | HCID 191066 | — |
| Reactant | Potassium methoxide | HCID 23664618 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21495671 | HCID 21495671 | 72.3% |
Reaction Steps
17.5 g of 89% potassium methylate were added under an inert atmosphere to a suspension of 7.5 g of 4-(3'-p-chlorobenzoyl-2'-methyl-phenyl)-butyric acid (Example V) in 75 ml of methanol and was then heated at 120°-130° C for 17 hours under pressure. After cooling to room temperature, the mixture was rinsed with water and the methanol was eliminated under reduced pressure. The residue was dissolved in water, treated hot with activated carbon, iced and filtered. The filtrate was acidified to a pH of 1 with hydrochloric acid and the precipitate formed was recovered by filtration, was washed with water until the wash water was neutral and dried. The residue was crystallized from isopropyl ether to obtain 5.35 g of 4-(3'-p-methoxybenzoyl-2'-methyl-phenyl)-butyric acid in the form of colorless crystals melting at 100° C and then 115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03995056 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-b982dcc69d5e4b6795014530bd0c032f |
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| Source note | uspto-grants-1976_11 |
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