Water → Succinanilic acid, 3'-(dihydroxyboryl)-

HRID 54629

反応式

HRID 54629 の反応式
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH2:3][CH2:2]1.[NH2:8][C:9]1[CH:10]=[C:11]([B:15]([OH:17])[OH:16])[CH:12]=[CH:13][CH:14]=1.O>N1C=CC=CC=1>[OH:16][B:15]([OH:17])[C:11]1[CH:10]=[C:9]([NH:8][C:1](=[O:7])[CH2:2][CH2:3][C:4]([OH:6])=[O:5])[CH:14]=[CH:13][CH:12]=1

参加物

5

実験手順

Succinic anhydride (5.00 grams, 0.05 mole) and (3-aminophenyl)boronic acid (7.75 grams, 0.05 mole) are dissolved in anhydrous pyridine (40 ml), and then allowed to stand overnight at room temperature. Water (20 ml) is added and the resulting solution allowed to stand for 1 hour. The product is then concentrated on a rotary evaporator at 85°-90° C. The resulting aqueous solution is Frozen in a dry-ice-acetone-slurry and lyophilized overnight. The lyophilized product is dissolved in water (50 ml) and acidified with concentrated HCl to approximately pH 1.0. The acidified solution is cooled in an ice bath for 1 hour, and the precipitate collected by filtration. The precipitate is recrystallized from boiling water (200 ml) and dried overnight in vacuo over NaOH pellets, to afford 8.60 grams (70% yield) of N-(3-dihydroxyborylphenyl)succinamic acid. Homogeneous by TLC (CHCl3 /CH3OH/CH3COOH; 60:35:5), Rf =0.5. Melting point 186°-188° C. The structure was confirmed by 300 MHz, 1H NMR spectrometry in d6 -DMSO.

後処理

  1. waitto stand for 1 hour
  2. concentrationThe product is then concentrated on a rotary evaporator at 85°-90° C
  3. temperatureThe resulting aqueous solution is Frozen in a dry-ice-acetone-slurry
  4. waitlyophilized overnight
  5. dissolutionThe lyophilized product is dissolved in water (50 ml)
  6. temperatureThe acidified solution is cooled in an ice bath for 1 hour
  7. filtrationthe precipitate collected by filtration
  8. customThe precipitate is recrystallized
  9. dry with materialdried overnight in vacuo over NaOH pellets

出典と根拠

ORDレコード
ord-1391736cb1c34508aaf57410193dacbf
出典データセット
uspto-grants-1997_04
特許番号
US05623055

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