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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 239845Erstellt: 24. Oktober 2026

Hydrochloric Acid → N-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamide

https://huagongshe.com/de/reaction/239845

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Iodobenzenesulfonyl chlorideHCID 7399—
Edukt2-Amino-5-chlorobenzophenoneHCID 12870—
LösungsmittelPyridineHCID 1049—
LösungsmittelTolueneHCID 1140—
ProduktN-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamideHCID 10028837—

Reaktionsschritte

To a magnetically stirred solution of 2-amino-5-chlorobenzophenone (1.62 g, 7.0 mmol) in dry pyridine (30 mL) was added dropwise a solution of pipsyl chloride in toluene (12 mL) and the reaction was stirred at ambient temperature. The reaction was added to cold (ice bath) 6M hydrochloric acid with stirring and the mixture was extracted with ethyl acetate (3×50 mL). The extracts were washed with water and with saturated aqueous NaCl. The organic layer was dried (MgSO4), filtered and concentrated to give a crystalline solid. The product was filtered, washed with hexane and dried (vacuum) to get white crystalline solid. 1H NMR (CDCl3) δ 9.63 (br s, 1H, NH), 7.75 (dm, 1H, J=8.8 Hz), 7.62 (tm, 1H, J=7.6 Hz), 7.56 (dm, 1H, J=7.6 Hz), 7.48 (m, 3H), 7.32 (m, 5H). MS: m/z 498.0 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642808B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-fb94709c1f074dc18b8ad86fd932c0bc
Quellennotizuspto-grants-2014_02