HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400619Generated: October 26, 2026
Sodium Hydroxide → 3-(5-Fluoro-2-methylphenyl)-3-methylbutanoic acid
https://huagongshe.com/reaction/400619
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,1,1-Trifluoro-4-(5-fluoro-2-methylphenyl)-4-methylpentan-2-one | HCID 20796120 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(5-Fluoro-2-methylphenyl)-3-methylbutanoic acid | HCID 58509552 | — |
Reaction Steps
A solution of 1,1,1-trifluoro-4-(5-fluoro-2-methylphenyl)-4-methylpentan-2-one (4.88 g, 18.6 mmol) was treated with sodium hydroxide solution (4 M in a mixture of 30% water in ethanol, 40 mL) at room temperature. The mixture was heated to 80° C. for 1 hour. After cooling to room temperature, the mixture was diluted with 100 mL of water and extracted with three 100 mL portions of diethyl ether. The aqueous layer was treated with 150 mL of ethyl acetate and the resulting mixture was treated with 6 M HCl dropwise until the solution had a pH of 2. The phases were separated and the aqueous layer was extracted with three 100 mL portions of ethyl acetate. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo to yield 3.92 g of 3-(5-fluoro-2-methylphenyl)-3-methylbutyric acid as an oil, which solidified upon standing and was used without further purification (quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741897B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-cbe7510bc25b49a5bf4c25d8a063843b |
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| Source note | uspto-grants-2014_06 |
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