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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 497261Erstellt: 23. Oktober 2026

Hydrochloric Acid → 4-Acetyl-2-fluorobenzene-1-sulfonamide

https://huagongshe.com/de/reaction/497261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSulfur DioxideHCID 1119—
EduktSodium NitrateHCID 24268—
Edukt1-(4-Amino-3-fluorophenyl)ethan-1-oneHCID 3018463—
KatalysatorCupric chloride dihydrateHCID 61482—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt4-Acetyl-2-fluorobenzene-1-sulfonamideHCID 2231696446,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 4-acetyl-2-fluoroaniline (5.0 g, 32.6 mmol, Krueger, G et al., Arzneim Forsch, 34, 11a, 1612 (1984)) in conc-HCl (24.0 mL), sodium nitrate (2.9 g, 42.4 mmol) in water (10 mL) was added at 0° C. After stirring for 1 h, the resultant yellow solution was added slowly to the suspension of copper (II) chloride dihydrate (1.7 g, 9.8 mmol) and sulfur dioxide (10 g, 156 mmol) in acetic acid (25 ml) at 0° C. The mixture was stirred for 30 min at 0° C. and poured into ice water (200 mL) and extracted with CH2Cl2 (80 mL×2). The extracts was cooled to 0° C. and 25% aqueous ammonia (70 mL) was added slowly and stirred for 1 h at room temperature. The mixture was concentrated and the residual solid was suspended with ether and collectted by filteration to give the title compound (3.3 g, 46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06949536B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-81a220ba26cf4e4593f7307de0d41507
Quellennotizuspto-grants-2005_09