Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782232Generated: October 30, 2026

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

https://huagongshe.com/reaction/1782232

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 numberUS07498337B2
Source datasetuspto-grants-2009_03
ORD IDord-35771c8ef4bf4af6a1e4fe3ca0060164
Source noteuspto-grants-2009_03