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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090631Generated: October 31, 2026

N-Methylmorpholine N-oxide monohydrate → 5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/2090631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methylmorpholine N-oxide monohydrateHCID 2724197—
Reactant[5-Bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methanolHCID 66924670—
CatalystHCID 178419074HCID 178419074—
SolventAcetonitrileHCID 6342—
Product5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 8623280571%

Reaction Steps

To a solution (80 mL) of [5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methanol (7.1 g) in acetonitrile were added tetra-n-propylammonium perruthenate (0.63 g), N-methylmorpholine N-oxide hydrate (4.2 g) and molecular sieves 4A powder (3.5 g), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Water was added to the residue, 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=4:1) to give the title compound as a colorless solid (yield 4.6 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436187B2
Source datasetuspto-grants-2013_05
ORD IDord-c242d90db214401c8bd99e0e52c28378
Source noteuspto-grants-2013_05