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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 224671Erstellt: 24. Oktober 2026

Tert-Butylamine → N-tert. butyl-4-,5-dimethylfuran-3-sulfonamide

https://huagongshe.com/de/reaction/224671

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-ButylamineHCID 6385—
EduktPhosphorus pentachlorideHCID 24819—
Edukt2,3-DimethylfuranHCID 34337—
Edukt5-Methyl-2-sulfamoyl-furan-3-carboxylic acidHCID 20471898—
Edukt4,5-Dimethyl-furan-2-sulfonic acid sodium saltHCID 88714704—
ProduktN-tert. butyl-4-,5-dimethylfuran-3-sulfonamideHCID 8673733134%

Reaktionsschritte

Analogous to the preparation of the 5-methyl-2-sulfamoyl-furan-3-carboxylic acid (see starting compound of Example 1), 2,3-dimethyl-furan [K. C. Rice and J. R. Dyer, J. Heterocycl. Chem. 12, 1325 (1975)] was converted with sulfur trioxide-pyridine complex into the 4,5-dimethyl-furan-2-sulfonic acid sodium salt and treated with phosphorus pentachloride and tert. butylamine. N-tert. butyl-4-,5-dimethyl-furan-3-sulfonamide was obtained with a yield of 34% of theory. M.p. 95°-96° C. (from petroleum ether).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04233333
Quelldatensatzuspto-grants-1980_11
ORD IDord-8b93a81753ca48d6b28337f1b76e719a
Quellennotizuspto-grants-1980_11