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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548198Generated: October 29, 2026

Sodium Hydroxide → 4-(3,5-Bis(trifluoromethyl)benzyloxy)-3-phenylbutanoic acid

https://huagongshe.com/reaction/548198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoateHCID 86624037—
SolventEthanolHCID 702—
Product4-(3,5-Bis(trifluoromethyl)benzyloxy)-3-phenylbutanoic acidHCID 86624038109.1%

Reaction Steps

Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoate (26.06 g, 60 mmol) was dissolved in ethanol (300 mL), a 2 mol/L aqueous solution of sodium hydroxide was added thereto and the mixture was stirred for 20 hours at room temperature. The solvent was evaporated in vacuo and the resulting residue was dissolved in water and acidified with 6 mol/L hydrochloric acid. The oily product separated out therefrom was extracted with chloroform and the organic layers were combined and washed with water and a saturated saline solution. After it was dried over anhydrous sodium sulfate, the solvent was evaporated in vacuo to give 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoic acid (26.60 g, 90%) as an oily product. 1H-NMR (DMSO-d6) δ: 2.56 (dd, J=8.4, 16.0 Hz, 1H), 2.73 (dd, J=6.4, 16.0 Hz, 1H), 3.35-3.40 (m, 1H), 3.63-3.66 (m, 2H), 4.64 and 4.66 (ABq, J=13.4 Hz, 2H), 7.19-7.25 (m, 1H), 7.27-7.31 (m, 4H), 7.88 (s, 2H), 7.98 (s, 1H), 12.09 (brs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939552B2
Source datasetuspto-grants-2011_05
ORD IDord-15bd7307ac574a6c814ce9446a0d1a27
Source noteuspto-grants-2011_05