Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234093Erstellt: 24. Oktober 2026

N-Hydroxysuccinimide → N-(3-dihydroxyboryl-phenyl)succinamic acid, succinimidyl ester

https://huagongshe.com/de/reaction/234093

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-HydroxysuccinimideHCID 80170—
EduktSuccinanilic acid, 3'-(dihydroxyboryl)-HCID 208171—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(3-dihydroxyboryl-phenyl)succinamic acid, succinimidyl esterHCID 8675020559,4%

Reaktionsschritte

N-(3-dihydroxyborylphenyl)succinamic acid (16.0 grams, 0.063 mole) is dissolved in dry DMF (80 ml). To the solution is added N,N-dicyclohexylcarbodiimide (14.3 grams, 0.069 mole) followed by N-hydroxysuccinimide (8.05 grams, 0.070 mole). The reaction is stirred overnight at room temperature. N,N-dicyclohexylurea is filtered from the solution, and the filtrate extracted with ethyl acetate (200 ml). The extract is washed with water (3×400 ml) and saturated NaCl (400 ml). The water wash was back-extracted with ethyl acetate (200 ml), the extracts combined, dried over anhydrous Na2SO4, and concentrated on a rotary evaporator to afford 12.5 grams (57% yield) of N-(3-dihydroxyboryl-phenyl)succinamic acid, succinimidyl ester. Purity estimated at 98% by TLC (CHCl3 /CH3OH/CH3COOH; 85:10:5), Rf =0.7. The structure was confirmed by 300 MHz, 1H NMR spectrometry in d6 -DMSO.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594111
Quelldatensatzuspto-grants-1997_01
ORD IDord-bc66482347ab48db8e084f4ecac9a460
Quellennotizuspto-grants-1997_01