HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012405Generated: October 25, 2026
N-Methylmorpholine N-oxide monohydrate → 5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde
https://huagongshe.com/reaction/1012405
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylmorpholine N-oxide monohydrate | HCID 2724197 | — |
| Reactant | [5-Bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methanol | HCID 66924670 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde | HCID 86232805 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977488B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-0db359eb06c84c0088818e2d022d1063 |
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| Source note | uspto-grants-2011_07 |
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