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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23820Erstellt: 24. Oktober 2026

Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- → 2,5-Dichloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide

https://huagongshe.com/de/reaction/23820

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)-HCID 11037—
EduktSodium cyanoborohydrideHCID 5003444—
EduktHydrochloride methanolHCID 21893726—
Edukt2,5-dichloro-N-(2-hydroxyimino-ethyl)-benzamideHCID 73987900—
LösungsmittelMethanolHCID 887—
Produkt2,5-Dichloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamideHCID 2259061240%

Reaktionsschritte

To a solution of 2,5-dichloro-N-(2-hydroxyimino-ethyl)-benzamide (0.72 g, 2.9 mmol) in MeOH (20 mL) under an argon atmosphere at 0° C. was added methyl orange (trace) followed by a saturated solution of MeOH/HCl until a persistent red color was observed. Sodium cyanoborohydride (0.22 g, 3.5 mmol) was dissolved in MeOH (5 mL) and was added sequentially with saturated MeOH/HCl over 0.5 h. The reaction mixture was stirred an additional 1 h and the MeOH was removed in vacuo. The residue was basidified with saturated Na2CO3 and extracted (7×25 mL) with dichloromethane/MeOH (9:1). The combined organic extracts were washed with brine, were dried (Na2SO4) and were concentrated. The residue was purified by flash chromatography (2%-5% MeOH/dichloromethane) to provide the title compound (0.29 g, 40%) as a white solid. 1H NMR (400 MHz, CD3OD): δ 7.53 (s, 1H); 7.44 (s, 2H); 3.56 (t, j=6.2 Hz, 2H); 3.06 (t, j=6.2 Hz, 2H). ESMS: M+H=249.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852882B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-82447eab617b430281efa9b577a3071a
Quellennotizuspto-grants-2005_02