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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599131Generated: October 31, 2026

Hydrogen Peroxide → (R)-2-[5-(4-Fluoro-2-trifluoromethyl-benzyloxy)-4'-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoic acid

https://huagongshe.com/reaction/599131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium SulfiteHCID 24437—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant4-Benzyl-3-{2-[5-(4-fluoro-2-trifluoromethyl-benzyloxy)-4'-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoyl}-oxazolidin-2-oneHCID 76587801—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-[5-(4-Fluoro-2-trifluoromethyl-benzyloxy)-4'-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoic acidHCID 5766731475.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-benzyl-3-{2-[5-(4-fluoro-2-trifluoromethyl-benzyloxy)-4′-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoyl}-oxazolidin-2-one (0.535 g, 0.78 mmol) in THF (9 mL) was added water (3 mL). The system was cooled to 0° C. To this cold solution was added LiOH.H2O (33 mg, 0.78 mmol) and 30% H2O2 (0.354 mL, 3.12 mmol,) and stirred at 0° C. for 20 min. The excess H2O2 was quenched by adding 1.5 M aqueous Na2SO3 solution (2.08 mL, 3.12 mmol) and stirred at room temperature for 5 min. The organic solvent was removed in vacuo. The resulting liquid was acidified to pH 2 by adding 1 N aqueous HCl solution. The aqueous layer was extracted with EtOAc (3×50 mL) and dried (MgSO4). The mixture was concentrated in vacuo to receive a crude mixture which was purified by ISCO silica gel column chromatography to yield (R)-2-[5-(4-Fluoro-2-trifluoromethyl-benzyloxy)-4′-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoic acid (310 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897643B2
Source datasetuspto-grants-2011_03
ORD IDord-278d49063dfa4f948af29fb64ed8381d
Source noteuspto-grants-2011_03