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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 812Erstellt: 23. Oktober 2026

Methyl iodide → N-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide

https://huagongshe.com/de/reaction/812

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktN-(tert-Butyl)-1H-pyrrole-3-sulfonamideHCID 19693846—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamideHCID 19693811—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of N-(1,1-dimethylethyl)-1H-pyrrole-3 -sulfonamide 9 g (0.044 mol) in 90 mL N,N-dimethylforamide was cooled to 15° C. under a nitrogen atmosphere. To this was added 3.2 mL (0.053 mol) of methyl iodide followed by 5.43 g (0.048 mol) of potassium t-butoxide. The mixture was warmed at ca. 60° C. for 2 hours then allowed to cool to room temperature and stirred for ca. 2 hours. The reaction mixture was diluted with ethyl acetate, washed three times with 1N HCl, once with brine, dried (MgSO4) and evaporated to an oily solid which was triturated with 5% diethyl ether/95% hexanes affording 6 g of the title compound as a beige solid, m.p. 134°-135° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723410
Quelldatensatzuspto-grants-1998_03
ORD IDord-c014829738084401b0a152f2e7cdf4bb
Quellennotizuspto-grants-1998_03