Ethyl 2-cyano-3-phenylpropanoate → Ethyl 3-amino-2-benzylpropanoate

HRID 727485

Reaktionsgleichung

Reaktionsgleichung von HRID 727485
[CH2:1]([CH:8]([C:14]#[N:15])[C:9]([O:11][CH2:12][CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>CCO.[Ni]>[NH2:15][CH2:14][CH:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C:9]([O:11][CH2:12][CH3:13])=[O:10]

Komponenten

4

Versuchsvorschrift

The resulting ethyl benzylcyanoacetate was dissolved in 200 ml of EtOH and hydrogenated over Raney nickel. After removal of the catalyst by filtration with suction and concentration, 8.2 . . . of oil were obtained, and chromatography over silica gel (EA to EA/MeOH 5/1) gave 5.5 g of ethyl 3-amino-2-benzylpropionate. This compound was reacted with Boc2O to give ethyl 2-benzyl-3-(tert.-butoxycarbonylamino)-propionate, which was hydrolyzed, and the product was coupled with H-Val-OMe by the PPA method. The resulting diastereomers were resolved by chromatography (toluene/diisopropyl ether 1/1).

Aufarbeitung

  1. customAfter removal of the catalyst
  2. filtrationby filtration
  3. concentrationwith suction and concentration, 8.2
  4. customof oil were obtained

Quellen und Nachweise

ORD-Eintrag
ord-90bd783a37ef46e9a04450fc5a2839c3
Quelldatensatz
uspto-grants-1998_01
Patentnummer
US05712417

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