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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426358Generated: October 30, 2026

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

https://huagongshe.com/reaction/426358

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 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 numberUS08106236B2
Source datasetuspto-grants-2012_01
ORD IDord-c8a8114657224298a2ce85601994e086
Source noteuspto-grants-2012_01