Reaktion #711522

ord-b080b29fbf0340c5b64a3c030870d7f6

Reaktionsgleichung

Oc1cccc(OCc2ccccc2)c1
3-(benzyloxy)phenol
CN(C)CCCl
2-chloro-N,N-dimethylethanamine
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CN(C)CCOc1cccc(OCc2ccccc2)c1
desired product
CN(C)CCOc1cccc(OCc2ccccc2)c1
2-(3-(benzyloxy)phenoxy)-N,N-dimethylethanamine

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe layers were separated
  2. 2
    ExtraktionThe aqueous layer was extracted with ethyl acetate
  3. 3
    Trocknenthe combined organic layers were dried over MgSO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated
  6. 6
    SonstigeThe residue was purified by flash chromatography (5% 7N NH; in methanol-dichloromethane)

Vorschrift

A solution of 3-(benzyloxy)phenol (2.002 g), 2-chloro-N,N-dimethylethanamine (1.459 g) in N,N-dimethylformamide (50 mL) was treated with cesium carbonate (3.91 g) and stirred at 50° C. overnight. The mixture was diluted with ethyl acetate and 1N aqueous NaOH and the layers were separated. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography (5% 7N NH; in methanol-dichloromethane) to give the desired product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09303025B2uspto-grants-2016_04