Reaktion #170124

ord-df8f8c4729084f1e89502c2b257a43f8

Reaktionsgleichung

BrCc1ccccc1
benzyl bromide
OC1CN(C(c2ccccc2)c2ccccc2)C1
1-diphenylmethylazetidin-3-ol
[H-].[Na+]
NaH
c1ccc(COC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
product
Ausbeute 24.3%
c1ccc(COC2CN(C(c3ccccc3)c3ccccc3)C2)cc1
3-(Benzyloxy)-1-(diphenylmethyl)azetidine
Ausbeute 24.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto warm to room temperature
  2. 2
    Temperaturthen heated to 80° C. overnight
  3. 3
    TemperaturThe reaction mixture was cooled
  4. 4
    Einengenthe mixture concentrated under reduced pressure
  5. 5
    SonstigeThe crude material was purified on column chromatography (eluent: Pentane/EtOAc, 95/5 to 70/30)

Vorschrift

To a solution of 1-diphenylmethylazetidin-3-ol (300 mg, 1.3 mmol) in DMF (2.6 mL) at 0° C. under nitrogen was added NaH (60% in oil, 56 mg, 1.4 mmol). The suspension was stirred for 0.5 h at 0° C. then treated with benzyl bromide (236 μL, 2.0 mmol). The mixture was allowed to warm to room temperature then heated to 80° C. overnight. The reaction mixture was cooled, acetic acid (20 drops) was added and the mixture concentrated under reduced pressure. The crude material was purified on column chromatography (eluent: Pentane/EtOAc, 95/5 to 70/30) to give the product (104 mg, 24%) as an orange oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846711B2uspto-grants-2014_09