Réaction #1285

ord-89c19946194d4a158a9cbb1375586293

Équation de réaction

O=N[O-].[Na+]
sodium nitrite
Cc1ccccc1
toluene
N[C@@H](Cc1ccccc1)C(=O)O
L-phenylalanine
[Br-].[K+]
potassium bromide
O=C(O)[C@@H](Br)Cc1ccccc1
(S)-α-Bromobenzenepropanoic acid

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionafter which the reaction mixture was extracted with ether (3×250 ml.)
  2. 2
    LavageThe combined organic extracts were washed with water (100 ml.) and brine (50 ml.)
  3. 3
    Séchagedried (anhydrous magnesium sulfate)
  4. 4
    Filtrationfiltered
  5. 5
    Autreevaporated to dryness
  6. 6
    Autredried in vacuo
  7. 7
    Autreto give 34.46 g

Mode opératoire

A solution of L-phenylalanine (30.0 g., 0.175 mole) and potassium bromide (73.5 g., 0.618 mole) in 2.5N sulfuric acid (365 ml.) was cooled down to 0° (ice-salt bath) and treated portionwise with sodium nitrite (19.3 g., 0.28 mole) over a period of 1.0 hour. Stirring was continued for 1.0 hour at 0° and at room temperature for 1.0 hour after which the reaction mixture was extracted with ether (3×250 ml.). The combined organic extracts were washed with water (100 ml.) and brine (50 ml.), dried (anhydrous magnesium sulfate), filtered, evaporated to dryness and dried in vacuo to give 34.46 g., of product; Rf =0.45 (toluene:acetic acid, 95:5).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723457uspto-grants-1998_03