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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268949Generated: October 30, 2026

Hydrogen Peroxide → (S)-3-(4-hydroxyphenyl)-2-(4-methylphenoxy)propionic acid

https://huagongshe.com/reaction/1268949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantLithium HydroxideHCID 3939—
ReactantSodium DithioniteHCID 24489—
Reactant(S)-4-Benzyl-3-[(S)-3-(4-hydroxyphenyl)-2-(4-methylphenoxy)propionyl]oxazolidin-2-oneHCID 69504567—
SolventMethanolHCID 887—
Product(S)-3-(4-hydroxyphenyl)-2-(4-methylphenoxy)propionic acidHCID 6950455982.4%

Reaction Steps

To a suspension of (S)-4-benzyl-3-[(S)-3-(4-hydroxyphenyl)-2-(4-methylphenoxy)propionyl]oxazolidin-2-one (6.50 g) obtained from Reference example 20(d) in methanol (80 ml) was added dropwise a mixed solution of an aqueous solution of lithium hydroxide (1N, 37.7 ml) and an aqueous solution of hydrogen peroxide (31%, 4.14 ml). The reaction solution was stirred for 1 hour at room temperature, then an aqueous solution (20 ml) of sodium hydrosulfite (6.56 g) was added thereto followed by stirring for 1 hour, and the resulting reaction solution was concentrated under reduced pressure. To the residue was added an aqueous solution of sodium hydroxide (1N), then the resulting alkaline solution was washed with dichloromethane and acidified by addition of hydrochloric acid. Ethyl acetate was added thereto, and the resulting solution was stirred and partitioned between ethyl acetate and water. The separated ethyl acetate layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was crystallized by addition of isopropyl ether and hexane to yield (S)-3-(4-hydroxyphenyl)-2-(4-methylphenoxy)propionic acid (3.38 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199139B2
Source datasetuspto-grants-2007_04
ORD IDord-ab281fd1f4864d35bde3cd6ad27a7231
Source noteuspto-grants-2007_04