Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402362Generated: November 1, 2026

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

https://huagongshe.com/reaction/2402362

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 the 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, the volatile solvents were substantially 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 numberUS08796335B2
Source datasetuspto-grants-2014_08
ORD IDord-c02992d21bef42cc9eebde9952dcfc77
Source noteuspto-grants-2014_08