Reaktion #497067

ord-536a936dba024c3ea51e58cd1bef98f8

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigequenched with aq. NaHCO3
  2. 2
    Extraktionthe resulting mixture was extracted with CH2Cl2
  3. 3
    TrocknenThe organic solution was dried over Na2SO4
  4. 4
    Einengenconcentrated
  5. 5
    SonstigePurification by flash column chromatography (silica gel, 40% EtOAc/heptane)

Vorschrift

To a solution of 1-Boc-3-aminoazetidine 1a (1.2 g, 6.98 mmol) and Et3N (2.4 mL, 17.3 mmol) in CH2Cl2 (70 mL) at 0° C. was added benzoyl chloride 1b (0.89 mL, 7.68 mmol). The reaction was kept at 0° C. for 3 h, quenched with aq. NaHCO3, and the resulting mixture was extracted with CH2Cl2. The organic solution was dried over Na2SO4 and concentrated. Purification by flash column chromatography (silica gel, 40% EtOAc/heptane) gave compound 1c (1.9 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08759533B2uspto-grants-2014_06