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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1426654Erstellt: 27. Oktober 2026

Benzenesulfonyl chloride → 5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/1426654

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
EduktSodium hydrideHCID 24758—
Edukt5-bromo-1H-pyrrole-3-carbaldehydeHCID 57831983—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 8623280585,5%

Reaktionsschritte

To a solution of 5-bromo-1H-pyrrole-3-carbaldehyde (3.50 g) in tetrahydrofuran (70 mL) was added sodium hydride (60% in oil, 1.21 g) at room temperature, and the mixture was stirred for 10 min. Benzenesulfonyl chloride (4.27 g) was added, and the mixture was further stirred for 1 hr, diluted with water, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→7:3) and crystallized from diisopropyl ether to give the title compound as colorless crystals (yield 5.4 g, 85%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08933105B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-65dd15020501426ebe740c5be79d578a
Quellennotizuspto-grants-2015_01