Réaction #52165

ord-a9b3277e1a1d4138a3507c1a34129fe5

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Concentrationthe reaction was concentrated in vacuo
  2. 2
    workup.DISSOLUTIONthe resulting oil dissolved in CH2Cl2 (25 ml)
  3. 3
    workup.STIRRINGAfter stirring for 3 h
  4. 4
    Filtrationthe reaction was filtered
  5. 5
    Concentrationconcentrated in vacuo
  6. 6
    AutreThe residue was purified by flash column chromatography on silica gel
  7. 7
    Lavageeluted with hexane/ethyl acetate (4:1)

Mode opératoire

To a solution of 2,3-dibromopropionyl chloride (5.00 g, 19.97 mmol) in THF (25 ml) at 0° C. was added dropwise benzyl alcohol (2.10 ml, 19.97 mmol). After stirring for 1 h, the reaction was concentrated in vacuo and the resulting oil dissolved in CH2Cl2 (25 ml) and treated with a solution of benzyl amine (2.20 ml, 19.97 mmol) and TEA (5.80 ml, 41.94 mmol) in CH2Cl2 (10 ml) at 0° C. After stirring for 3 h, the reaction was filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluted with hexane/ethyl acetate (4:1) to afford N-benzyl-aziridine-2-carboxylic acid, benzyl ester as a colorless oil (2.35 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06855708B2uspto-grants-2005_02