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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476081Generated: November 4, 2026

Sodium Hydroxide → (3R)-2-(4-ethylphenyl)-4,4,4-trifluoro-3-methylbutanoic acid

https://huagongshe.com/reaction/1476081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl(3R)-2-(4-ethylphenyl)-4,4,4-trifluoro-3-methylbutanoateHCID 58288230—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(3R)-2-(4-ethylphenyl)-4,4,4-trifluoro-3-methylbutanoic acidHCID 58288296—

Reaction Conditions

Temperature40 °C

Reaction Steps

3.0 g of ethyl (3R)-2-(4-ethylphenyl)-4,4,4-trifluoro-3-methylbutanoate (purity about 88%, about 9.16 mmol; diastereomer mixture) were dissolved in a mixture of in each case 12.4 ml of methanol, THF and water, and 5.49 g (137.35 mmol) of sodium hydroxide were added a little at a time. The reaction mixture was stirred at 40° C. for 9 h. After cooling, most of the volatile solvents were removed under reduced pressure and the residue was diluted with water. The mixture was acidified by addition of hydrochloric acid, and the aqueous phase was extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated under reduced pressure, and the residue was dried under high vacuum. This gave 2.61 g of the title compound as a crude product which was not purified any further (diastereomer ratio about 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018414B2
Source datasetuspto-grants-2015_04
ORD IDord-e4c9d3de5c234443be8060b24f82bdb5
Source noteuspto-grants-2015_04