(3S)-3-hydroxy-3-phenylpropanenitrile → (1S)-3-amino-1-phenylpropan-1-ol

HRID 1760083Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1760083
[C:1]1([C@@H:7]([OH:11])[CH2:8][C:9]#[N:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>C1COCC1>[C:1]1([C@@H:7]([OH:11])[CH2:8][CH2:9][NH2:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Komponenten

3

Versuchsvorschrift

To a THF solution of (S)-3-phenyl-3-hydroxypropanenitrile was slowly added THF solution of borane dimethyl sulfide complex at room temperature. Methyl sulfide was then distilled from the reaction vessel and the resulting THF solution refluxed for 2.5 h. After cooling to room temperature methanolic HCl was added to the reaction mixture. Methanol and methyl borate were removed by distillation and the reaction mixture neutralized with sodium hydroxide (5N). Extraction of the mixture with dichloromethane,followed by concentration provided the crystalline (S)-3-phenyl-3-hydroxypropylamine.

Aufarbeitung

  1. customat room temperature
  2. distillationMethyl sulfide was then distilled from the reaction vessel
  3. temperaturethe resulting THF solution refluxed for 2.5 h
  4. additionwas added to the reaction mixture
  5. customMethanol and methyl borate were removed by distillation
  6. extractionExtraction of the mixture with dichloromethane,followed
  7. concentrationby concentration

Quellen und Nachweise

ORD-Eintrag
ord-6e2ece804d7d4ca8a8ffb642556a2c8b
Quelldatensatz
uspto-grants-2005_01
Patentnummer
US06838581B2

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