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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55301Erstellt: 24. Oktober 2026

Benzenesulfonamide → 4-Iodo-N-(phenylsulfonyl)benzamide

https://huagongshe.com/de/reaction/55301

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonamideHCID 7370—
Edukt4-Iodobenzoic acidHCID 12085—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Iodo-N-(phenylsulfonyl)benzamideHCID 448683140,4%

Reaktionsschritte

5 g of 4-iodobenzoic acid is added to a solution of 3.3 g of benzenesulfonamide, 2.68 g of 4-dimethylaminopyridine and 4.04 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide in 100 ml of dichloromethane, and the suspension is stirred for 18 hours at room temperature. The reaction mixture is diluted with 400 ml of dichloromethane, washed in succession with 400 ml portions of 10% hydrochloric acid, water and saturated common salt solution, the organic phase is dried on sodium sulfate and concentrated by evaporation. The residue is suspended in diethyl ether/ethyl acetate=1/1, and the crystallizate is suctioned off. 3.15 g of N-benzenesulfonyl-4-iodobenzoic acid amide of melting point 192°-193° C. is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624943
Quelldatensatzuspto-grants-1997_04
ORD IDord-b52ab99c986e4c808f849a844c91cd95
Quellennotizuspto-grants-1997_04