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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 816Erstellt: 23. Oktober 2026

Hydrochloric Acid → N-(1,1-Dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamide

https://huagongshe.com/de/reaction/816

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethyl DisulfideHCID 12232—
EduktN-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamideHCID 19693811—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(1,1-Dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamideHCID 1969381458,8%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 6.48 g (30 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 150 mL THF under nitrogen atmosphere cooled to -78° C. was added dropwise at such a rate as to keep the temperature below -65° C. 25.52 mL (61.5 mmol) 2.41M n-butyllithium in hexanes. The reaction was stirred at -78° C. for ca. 30 minutes. To the reaction mixture was added 2.97 mL (33 mmol) of dimethyldisulfide in one portion and the resulting reaction mixture was allowed to warm to room temperature and stir for ca. 1.5 hours. The reaction mixture was cooled to 0° C. and acidified with 1N HCl. The THF phase was separated washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue was chromatographed on silica (20% ethyl acetate/80% hexanes) affording 4.63 g of the title compound as an off white solid, m.p. 116°-119° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723410
Quelldatensatzuspto-grants-1998_03
ORD IDord-ec291f168e3d4ab6bc17d0209ef33361
Quellennotizuspto-grants-1998_03