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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992434Generated: November 1, 2026

Hydrogen Peroxide → 2-(R)-(3,4-Dihydro-1H-benzo[4,5]thieno[2,3-c]pyridine-2-sulfonylmethyl)-3-methyl-butyric acid

https://huagongshe.com/reaction/992434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium SulfiteHCID 24437—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant4(R)-Benzyl-3-[2-(R)-(3,4dihydro-1H-benzo[4,5]thieno[2,3-c]pyridine-2-sulfonylmethyl)-3-methyl-butanoyl]-oxazolidin-2-oneHCID 22888282—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(R)-(3,4-Dihydro-1H-benzo[4,5]thieno[2,3-c]pyridine-2-sulfonylmethyl)-3-methyl-butyric acidHCID 1027033587.6%

Reaction Steps

Hydrogen peroxide (30% aqueous, 0.15 ml) was added to a solution of 4(R)-benzyl-3-[2-(R)-(3,4-dihydro-1H-benzo[4,5]thieno[2,3-c]pyridine-2-sulfonylmethyl)-3-methyl-butanoyl]-oxazolidin-2-one (180 mg) in tetrahydrofuran (5 ml) at 0° C., followed by a solution of lithium hydroxide monohydrate (30 mg) in water (3 ml). The reaction was stirred for 16 h, allowing to warm slowly to room temperature. A solution of sodium sulfite (200 mg) in water (5 ml) was added then the mixture was evaporated under reduced pressure. The aqueous residue was washed with diethyl ether (20 ml), acidified with citric acid and extracted with ethyl acetate (2×30 ml). The combined extracts were washed with brine (30 ml), dried (MgSO4), filtered and evaporated under reduced pressure to give the title compound (110 mg) in crude form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469020B2
Source datasetuspto-grants-2002_10
ORD IDord-ebb8c583561540cba3c6d8267b77d1c0
Source noteuspto-grants-2002_10