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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54630Generated: October 26, 2026

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

https://huagongshe.com/reaction/54630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxysuccinimideHCID 80170—
ReactantSuccinanilic acid, 3'-(dihydroxyboryl)-HCID 208171—
SolventDimethylformamideHCID 6228—
ProductN-(3-dihydroxyboryl-phenyl)succinamic acid, succinimidyl esterHCID 8675020559.4%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05623055
Source datasetuspto-grants-1997_04
ORD IDord-5bd05ed4d0314ac18a7a1784e9f7d005
Source noteuspto-grants-1997_04