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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525569Generated: October 26, 2026

Sodium Hydroxide → 4-Cyano-3-(4-fluorophenyl)-4-(3-fluorophenyl)butanoic acid

https://huagongshe.com/reaction/1525569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-cyano-3-(p-fluorophenyl)-4-(m-fluorophenyl)butyrateHCID 14838737—
SolventMethanolHCID 887—
Product4-Cyano-3-(4-fluorophenyl)-4-(3-fluorophenyl)butanoic acidHCID 14838739—

Reaction Conditions

Temperature25 °C

Reaction Steps

Under protective gas (Ar), 10 ml of 2 molar aqueous sodium hydroxide solution were added to 1.75 g (5.55 mmol) of methyl 4-cyano-4-(3-fluorophenyl)-3-(4-fluorophenyl)butanoate in 50.0 ml of methanol, and the mixture was stirred at 25° C. for 8 h. The methanol was removed under reduced pressure. The residue was acidified with concentrated hydrochloric acid (pH=3) and extracted three times with in each case 15 ml of dichloromethane. The combined organic phases were dried over sodium sulphate and the solvent was removed under reduced pressure. This gave 1.62 g (96.9% of theory) of the title compound in the form of colourless crystals (erythro:threo=49:51, comparison of the multiplets in the 1H-NMR in CDCl3 at 2.60 and 2.85 ppm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09084425B2
Source datasetuspto-grants-2015_07
ORD IDord-c254525f84dc4932a5ad51d1db38347b
Source noteuspto-grants-2015_07