Reaktion #64795

ord-2d03759392e14e04aca18497b4e5b596

Reaktionsgleichung

C[Si](C)(C)N(C(=O)C(F)(F)F)[Si](C)(C)C
Bis (trimethylsilyl)trifluoroacetamide
N#CC[C@H](N)C(=O)O
(αS)-amino-3-cyanopropanoic acid
O=C(Cl)OCc1ccccc1
Benzylchloroformate
N#CC[C@H](NC(=O)OCc1ccccc1)C(=O)O
(2S)-[[(Phenylmethoxy)carbonyl]amino]-3cyanopropanoic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe reaction mixture was stirred overnight
  2. 2
    Einengenconcentrated in vacuo
  3. 3
    workup.DISSOLUTIONdissolved in ethyl acetate (200 mL)
  4. 4
    WaschenThe organic solution was washed with water (2 x) and brine
  5. 5
    Trocknendried (Na2SO4)
  6. 6
    Einengenconcentrated in vacuo
  7. 7
    SonstigeCrystallization from isopropyl ether
  8. 8
    Sonstigeyielded 3.82 g

Vorschrift

Bis (trimethylsilyl)trifluoroacetamide (9.4 mL, 35 mmol.) was added to a suspension of (αS)-amino-3-cyanopropanoic acid (2.0 g., 17.5 mmol.) in 10 mL of dry acetonitrile and the reaction mixture was stirred for 3 hours. Benzylchloroformate (2.5 mL, 17.5 mmol) was added, the reaction mixture was stirred overnight, concentrated in vacuo, and dissolved in ethyl acetate (200 mL). The organic solution was washed with water (2 x) and brine, dried (Na2SO4), and concentrated in vacuo. Crystallization from isopropyl ether yielded 3.82 g. of the title A product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05414013uspto-grants-1995_05