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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665258Generated: October 25, 2026

Hydrochloric Acid → 3-(2',4',5'-Trifluoro-biphenyl-4-yloxymethyl)-benzoic acid

https://huagongshe.com/reaction/1665258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant3-(2',4',5'-Trifluoro-biphenyl-4-yloxymethyl)-benzoic acid methyl esterHCID 67150368—
SolventWaterHCID 962—
Product3-(2',4',5'-Trifluoro-biphenyl-4-yloxymethyl)-benzoic acidHCID 5827119098.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 3-(2′,4′,5′-trifluoro-biphenyl-4-yloxymethyl)-benzoic acid methyl ester (18.96 g, 50.92 mmol) in inhibitor free THF (100 mL) was treated with a near solution of lithium hydroxide monohydrate (8.4 g, 200.2 mmol) in water (100 mL) at room temperature and heated at 60° C. for 4 h. The reaction mixture was cooled, diluted with water, acidified with aq. 2N HCl and extracted with ethyl acetate. The organic layers were combined, washed with 1/1 water/brine, brine, dried (MgSO4), filtered and concentrated to give 3-(2′,4′,5′-trifluoro-biphenyl-4-yloxymethyl)-benzoic acid (17.89 g, 98.0%) as an off white solid. LC-MS (ES) calculated for C20H13F3O3, 358.32; found m/z 357 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039495B2
Source datasetuspto-grants-2011_10
ORD IDord-d28e22108c1b4342b78a2654a05c9e8d
Source noteuspto-grants-2011_10