Réaction #40341

ord-d99e3ad127f8439ba0849a80a747879b

Équation de réaction

CCOC(=O)CNCc1ccccc1
N-benzylglycine ethyl ester
CCOC(=O)CCCCBr
5-bromovaleric acid ethyl ester
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOC(=O)CN(CCCCC(=O)O)Cc1ccccc1
5-(benzyl-ethoxycarbonylmethyl-amino)-pentanoic acid
Rendement 30.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction is quenched with saturated aqueous ammonium chloride solution, and extraction
  2. 2
    SéchageAfter drying over sodium sulphate the combined organic phases
  3. 3
    Concentrationare concentrated by evaporation

Mode opératoire

N-benzylglycine ethyl ester (1.87 ml) and 5-bromovaleric acid ethyl ester (1.92 ml) are dissolved in dimethylformamide (100 ml) and stirred in the presence of potassium carbonate (1.66 g) for 2 days at room temperature. The reaction is quenched with saturated aqueous ammonium chloride solution, and extraction is carried out with ethyl acetate. After drying over sodium sulphate the combined organic phases are concentrated by evaporation. From the obtained residue, 5-(benzyl-ethoxycarbonylmethyl-amino)-pentanoic acid is isolated in a yield of 30% by chromatography using silica gel (ethyl acetate/heptane 1:5).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07727979B2uspto-grants-2010_06