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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226548Generated: October 29, 2026

Water → (5-Benzyloxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid

https://huagongshe.com/reaction/226548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl [5-benzyloxy-4'-(trifluoromethyl)biphenyl-3-yl]acetateHCID 24771790—
SolventTetrahydrofuranHCID 8028—
Product(5-Benzyloxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acidHCID 1150191294%

Reaction Steps

To a solution of (5-benzyloxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester (120 g, 0.29 mol) in THF (1.2 L) was added water (240 mL), LiOH.H2O (16 g, 0.32 mol) and the resulting mixture was stirred at room temperature for 16 h. The solution was filtered and concentrated in vacuo to remove THF. The resulting thick liquid was acidified to pH 2 by adding 2N aqueous HCl solution and the white suspension was mechanically stirred for 1 h at room temperature. The wet white product was recovered after filtration and dissolved in EtOAc (500 mL). The organic layer was separated from water, dried (MgSO4) and concentrated in vacuo to obtain (5-benzyloxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid (105 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557244B2
Source datasetuspto-grants-2009_07
ORD IDord-3dd23bca1b5b4f94a80a5f5a960991bc
Source noteuspto-grants-2009_07