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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070471Generated: November 2, 2026

Sodium Thiosulfate → 5-[2-(methylsulfonyl)phenyl]-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/2070471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-[2-(methylthio)phenyl]-1H-pyrrole-3-carbaldehydeHCID 86630988—
SolventEthyl AcetateHCID 8857—
Product5-[2-(methylsulfonyl)phenyl]-1H-pyrrole-3-carbaldehydeHCID 8663099178%

Reaction Steps

To a solution of 5-[2-(methylthio)phenyl]-1H-pyrrole-3-carbaldehyde (100 mg) in ethyl acetate (5 mL) was added 3-chloroperbenzoic acid (318 mg) under ice-cooling. After stirring at room temperature for 3 hr, a saturated sodium thiosulfate aqueous solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=1:1→1:3) to give the title compound as pale-yellow crystals (yield 88.9 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299261B2
Source datasetuspto-grants-2012_10
ORD IDord-cc966e5eb04d4a28a419341a653c3b3c
Source noteuspto-grants-2012_10