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HRID 1873448Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1873448
[C:1]([C@@H:3]([CH2:8][CH:9]([CH3:11])[CH3:10])[CH2:4][C:5]([O-:7])=[O:6])#[N:2].[K+].O.[OH-].[K+].[H][H]>[Ni].C(O)(C)C>[NH2:2][CH2:1][C@@H:3]([CH2:8][CH:9]([CH3:11])[CH3:10])[CH2:4][C:5]([OH:7])=[O:6]

Komponenten

7

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A mixture of potassium (S)-3-cyano-5-methylhexanoate (20 g, 103.5 mmol), water (50 mL), 45% KOH (12 g), isopropanol (12 g), and Raney Nickel were shaken overnight in a Parr Shaker under 50 psi of hydrogen. The mixture was filtered, heated to approximately 50° C., treated with acetic acid (6.5 mL) and stirred overnight at room temperature. The mixture was then adjusted to slightly above pH 7 with 45% KOH and concentrated under vacuum to remove most of the isopropanol. Isopropanol (20 mL) was added to the mixture, which was then acidified with acetic acid, stirred overnight at room temperature, and filtered to give 4.3 g of (S)-3-aminomethyl-5-methylhexanoic acid as a white crystalline solid. The enantiomeric purity was determined to be 100% e.e. by preparing a derivative of (S)-3-aminomethyl-5-methylhexanoic acid using Marfey's reagent (Nα-(2,4-dinitro-5-fluorophenyl)-L-alaninamide) and analyzing by HPLC on a BDS Hypersil C18 column (250×4.6 mm, 5μ) eluted with acetonitrile:1% triethylamine (pH 3) (38:62, v/v).

Aufarbeitung

  1. filtrationThe mixture was filtered
  2. additiontreated with acetic acid (6.5 mL)
  3. concentrationconcentrated under vacuum
  4. customto remove most of the isopropanol
  5. additionIsopropanol (20 mL) was added to the mixture, which
  6. stirringstirred overnight at room temperature
  7. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-41d4326f2603483e965c48051c50215c
Quelldatensatz
uspto-grants-2012_11
Patentnummer
US08304252B2

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