Sulfuric Acid → 3-Maleimidophenyl boronic acid

HRID 54631

반응식

HRID 54631 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([B:8]([OH:10])[OH:9])[CH:5]=[CH:6][CH:7]=1.COC(N1[C:19](=[O:20])[CH:18]=[CH:17][C:16]1=[O:21])=O.OS(O)(=O)=O>C([O-])(O)=O.[Na+].O>[C:16]1(=[O:21])[N:1]([C:2]2[CH:3]=[C:4]([B:8]([OH:10])[OH:9])[CH:5]=[CH:6][CH:7]=2)[C:19](=[O:20])[CH:18]=[CH:17]1

참가 물질

6

반응물 3

HCID 1118Sulfuric AcidHCID 922693-Aminophenylboronic acidHCID 580610N-(Methoxycarbonyl)maleimide

생성물 1

HCID 224930233-Maleimidophenyl boronic acid수율 64.1%

시약·촉매·용매 2

HCID 962Water용매HCID 516892Sodium Bicarbonate용매

반응 조건

온도
0 °C

실험 절차

(3-Aminophenyl)boronic acid (1.26 grams, 0.01 mole) is dissolved in saturated NaHCO3 (50 ml) by briefly heating the mixture on a hot plate. The solution is cooled in an ice bath to approximately 0° C., and N-methoxycarbonylmaleimide (1.55 grams, 0.01 mole) added with vigorous stirring. After 10 min. the solution is diluted with water (200 ml) and then stirred at room temperature for 30 to 40 min. The pH is adjusted to approximately 5.5 by addition of 1M H2SO4, and the precipitate collected by filtration. The precipitate is washed with 1M H2SO4 (2×50 ml), and then dried overnight in vacuo over NaOH pellets to afford 1.39 grams (64% yield) of (3-maleimidophenyl)boronic acid. The structure was confirmed by 300 MHz, 1H NMR spectrometry in d6 -DMSO.

후처리

  1. temperatureby briefly heating the mixture on a hot plate
  2. filtrationthe precipitate collected by filtration
  3. washThe precipitate is washed with 1M H2SO4 (2×50 ml)
  4. dry with materialdried overnight in vacuo over NaOH pellets

출처 및 근거

ORD 기록
ord-8ed6c8aa8b684581b325a3620b1803c8
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05623055

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