Reaktion #64875

ord-da71adb801284935aabd431835879a32

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe resulting suspension is concentrated
  2. 2
    workup.ADDITION500 ml of diethyl ether are added
  3. 3
    Filtrationthe reaction mixture is then filtered
  4. 4
    Einengenthe tiltrate is concentrated
  5. 5
    SonstigePurification of the crude product by means of column chromatography

Vorschrift

46.4 g of hydrazine-N,N'-dicarboxylic acid di-tert-butyl ester, 69.0 g of potassium carbonate, 3.3 g of potassium iodide, 20 ml of tetrabutylammonium fluoride (1 molar solution in tetrahydrofuran) and 21 ml of epibromohydrin are boiled under reflux for 48 hours in 400 ml of ethyl methyl ketone. The resulting suspension is concentrated, and 500 ml of diethyl ether are added thereto; the reaction mixture is then filtered and the tiltrate is concentrated. Purification of the crude product by means of column chromatography yields 27.1 g of the desired 4-hydroxy-pyrazolidine-N,N'-dicarboxylic acid di-tert-butyl ester in the form of white crystals; m.p. 100°-102° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05416065uspto-grants-1995_05