4-Aminophenol → 2,4-Diacetoxy-N-[3-[(4-hydroxyphenyl)amino]-3-oxopropyl]-3,3-dimethylbutanamide

HRID 892879Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 892879
C(N=C=NCCCN(C)C)C.[C:12]([O:15][CH:16]([C:25]([CH3:32])([CH3:31])[CH2:26][O:27][C:28](=[O:30])[CH3:29])[C:17]([NH:19][CH2:20][CH2:21][C:22]([OH:24])=O)=[O:18])(=[O:14])[CH3:13].[CH:33]1[C:38]([NH2:39])=[CH:37][CH:36]=[C:35]([OH:40])[CH:34]=1>C(Cl)Cl>[C:12]([O:15][CH:16]([C:25]([CH3:32])([CH3:31])[CH2:26][O:27][C:28](=[O:30])[CH3:29])[C:17]([NH:19][CH2:20][CH2:21][C:22]([NH:39][C:38]1[CH:33]=[CH:34][C:35]([OH:40])=[CH:36][CH:37]=1)=[O:24])=[O:18])(=[O:14])[CH3:13]

Komponenten

5

Versuchsvorschrift

1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (2.30 g) was added to a solution of 3.03 g of 3-[N-(2,4-diacetoxy-3,3-dimethyl-1-oxobutyl)amino]propionic acid and 2.18 g of p-aminophenol in 50 ml of methylene chloride, and the mixture was stirred for one night. After completion of the reaction, the reaction mixture was washed with water, and dried over anhydrous sodium sulfate. After removing the solvent by evaporation, the residue obtained was purified by silica gel column chromatography to obtain 1.92 g of the objective compound was obtained as a residue (yield: 50%).

Aufarbeitung

  1. customAfter completion of the reaction
  2. washthe reaction mixture was washed with water
  3. dry with materialdried over anhydrous sodium sulfate
  4. customAfter removing the solvent
  5. customby evaporation
  6. customthe residue obtained
  7. customwas purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-29ebae54edf34cfdbcc7eb7763d0fa8a
Quelldatensatz
uspto-grants-1992_06
Patentnummer
US05120738

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