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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 658596Erstellt: 25. Oktober 2026

Furfurylamine → 4-[(Furan-2-ylmethyl)sulfamoyl]benzoic acid

https://huagongshe.com/reaction/658596

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFurfurylamineHCID 3438—
EduktSulfuryl chlorideHCID 24648—
Edukt4-(Chlorosulfonyl)benzoic acidHCID 82385—
LösungsmittelAcetoneHCID 180—
Produkt4-[(Furan-2-ylmethyl)sulfamoyl]benzoic acidHCID 68152568,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-(Chlorosulfonyl)benzoic acid (5.0 g, 22.7 mmol) was added in three portions over a 10 minute period to a stirring solution of furfuryl amine (6.6 g, 68 mmol) in acetone (200 mL) cooled to 0° C. via an ice water bath. After addition of the sulfonyl chloride was complete the ice bath was removed and the solution was stirred for 1 hour at ambient temperature. The mixture was concentrated and subjected to silica gel chromatography (90% ethyl acetate, 8% hexanes and 2% acetic acid) to afford 4.4 of 4-(N-(furan-2-ylmethyl)sulfamoyl)benzoic acid (4.4 g, 68%) as a white solid. 1H NMR (DMSO-d6, 400 MHz): 4.04 (d, 2H, J=6 Hz), 6.13 (d, 1H, J=3.2 Hz), 6.25 (m, 1H), 7.43 (m, 1H), 7.83 (d, 2H, J=8.4 Hz), 8.05 (d, 2H, J=8.4 Hz), 8.36 (t, 1H, J=6 Hz), 13.4 (bs, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08076491B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-812f233a29c64eb9ae8bcdaef2c8a178
Quellennotizuspto-grants-2011_12