Ethanol → 3-[(3,5-Dimethylphenyl)amino]propanoic acid

HRID 1531985Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1531985
[CH3:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([CH3:13])[CH:12]=1)[NH:5][CH2:6]CC#N.[OH-:14].[Na+].[CH2:16]([OH:18])[CH3:17]>O>[CH3:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([CH3:13])[CH:12]=1)[NH:5][CH2:6][CH2:17][C:16]([OH:14])=[O:18]

Komponenten

5

Edukt 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 2926323-[(3,5-Dimethylphenyl)amino]propanenitrile

Produkt 1

HCID 24348423-[(3,5-Dimethylphenyl)amino]propanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

β-(3,5-Dimethylanilino)propionitrile (4.5 g) was dissolved in ethanol (50 ml), and a solution of NaOH (5.1 g) in water (25 ml) was added, which was followed by refluxing for 4 hr. The solvent was evaporated under reduced pressure. 2N Hydrochloric acid was added to adjust the residue acidic, and the mixture was washed with chloroform (100 ml). The aqueous layer was concentrated to about 20 ml and allowed to stand. The precipitated crystals were collected by filtration and dried to give 4.0 g of β-(3,5-dimethylanilino)propionic acid.

Aufarbeitung

  1. temperatureby refluxing for 4 hr
  2. customThe solvent was evaporated under reduced pressure
  3. addition2N Hydrochloric acid was added
  4. washthe mixture was washed with chloroform (100 ml)
  5. concentrationThe aqueous layer was concentrated to about 20 ml
  6. filtrationThe precipitated crystals were collected by filtration
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-a255f76d6b4f4bff9e161139272c3390
Quelldatensatz
uspto-grants-2001_03
Patentnummer
US06200988B1

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