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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,1,1-Trifluoro-4-(5-fluoro-2-methylphenyl)-4-methylpentan-2-oneHCID 20796120—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-(5-Fluoro-2-methylphenyl)-3-methylbutanoic acidHCID 58509552—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-cbe7510bc25b49a5bf4c25d8a063843b
Source noteuspto-grants-2014_06