Réaction #2358505

ord-86231e5925954f78a659095389894bad

Équation de réaction

CC(C)C(N)C(=O)O
DL-valine
C[C@H](NC(=O)c1ccccc1)C(=O)O
N-benzoyl-L-alanine
CC(C)[C@H](N)C(=O)O.C[C@H](NC(=O)c1ccccc1)C(=O)O
L-valine N-benzoyl-L-alanine
Rendement 86.4%

Réactifs

Aucun

Solvants

Conditions de réaction

Température
95°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreto form a clear solution, which
  2. 2
    Températurewas cooled slowly
  3. 3
    TempératureWhen the solution was cooled to room temperature after 2 hours
  4. 4
    Autrethe precipitated crystals were separated by filtration
  5. 5
    Lavagewashed with 50 mL of deionized water
  6. 6
    Autredried

Mode opératoire

Twenty four grams of DL-valine and 19.3 g of N-benzoyl-L-alanine were suspended in 200 mL of deionized water. The suspension was heated to 95° C. to form a clear solution, which was cooled slowly. When the solution was cooled to room temperature after 2 hours, the precipitated crystals were separated by filtration, washed with 50 mL of deionized water, and dried to obtain 26.8 g of crystalline L-valine N-benzoyl-L-alanine complex (L-valine to N-benzoyl-L-alanine molar ratio of 1:1).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09120722B1uspto-grants-2015_09