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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23823Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/23823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)-HCID 11037—
EduktSodium cyanoborohydrideHCID 5003444—
EduktHydrochloride methanolHCID 21893726—
Edukt5-bromo-2-chloro-N-(2-hydroxyimino-ethyl)-benzamideHCID 73987902—
LösungsmittelMethanolHCID 887—
Produkt5-Bromo-2-chloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamideHCID 2259061035%

Reaktionsschritte

To a solution of 5-bromo-2-chloro-N-(2-hydroxyimino-ethyl)-benzamide (2 g, 6.9 mmol) in MeOH (75 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 (0.52 g, 8.2 mmol) was dissolved in MeOH (10 mL) and was added sequentially with saturated MeOH/HCl over 0.5 h. The reaction mixture was stirred an additional 2 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 to provide the title compound (0.7 g, 35%) as a white solid. ESMS: M+H=293.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852882B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-e20624abd66b4a55a6829ef35c4f7191
Quellennotizuspto-grants-2005_02