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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234093생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/234093

반응식

참여 물질

역할이름HCID투입량
반응물N-HydroxysuccinimideHCID 80170—
반응물Succinanilic acid, 3'-(dihydroxyboryl)-HCID 208171—
용매DimethylformamideHCID 6228—
생성물N-(3-dihydroxyboryl-phenyl)succinamic acid, succinimidyl esterHCID 8675020559.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594111
출처 데이터셋uspto-grants-1997_01
ORD IDord-bc66482347ab48db8e084f4ecac9a460
출처 메모uspto-grants-1997_01