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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629755Generated: October 30, 2026

Hydrogen Peroxide → HCID 86726357, compound

https://huagongshe.com/reaction/629755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantLithium HydroxideHCID 3939—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86726358HCID 86726358—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86726357HCID 86726357—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (4S)-3-[(2S,3S)-2-azido-3-(3,5-difluorophenyl)-3-(4-fluorophenyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one (3.1 g, 6.7 mmol) in 45 mL of THF and 15 mL of water was cooled to 0° C. in an ice-water bath. To the stirred solution was added hydrogen peroxide (2.7 mL of a 30% solution in water, 27 mmol) and LiOH (0.32 g, 13 mmol), and the mixture was stirred at 0° C. for 45 min. The reaction was quenched by the addition of a solution of sodium sulfite (3.4 g, 27 mmol) in 20 mL of water, followed by 67 mL of a 0.5 M solution of aqueous NaHCO3 (33 mmol). The stirred mixture was warmed to ambient temperature and most of the THF was removed in vacuo. The aqueous mixture was extracted with two portions of CH2Cl2 to remove the chiral auxiliary. The aqueous phase was then acidified to pH 1 with the addition of 6 N HCl and extracted with two portions of EtOAc. The combined EtOAc layers were dried (MgSO4), filtered, and the solvent was removed in vacuo to give a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-9f325c4e83ad4ea6b9c87281355ff7e6
Source noteuspto-grants-2016_04