Reaktion #48290

ord-8139b49a9c4945e694dea03a4c0b2ea9

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe reaction stirred an additional 1 h at 0° C
  2. 2
    workup.STIRRINGthe suspension stirred 30 min
  3. 3
    ExtraktionThe solution was extracted with EtOAc (3×400 mL)
  4. 4
    Waschenthe combined organic layers washed with H2O (500 mL), saturated NaCl (500 mL)
  5. 5
    Trocknendried (Na2SO4)
  6. 6
    Einengenconcentrated in vacuo

Vorschrift

To a solution of 6-bromopyridin-3-ol (25 g, 144 mmol) in DMF (300 mL) at 0° C. under N2 is added portionwise NaH (5.7 g, 144 mmol) over 5 min. The reaction was stirred 1 h, then chloro(methoxy)methane (12 g, 144 mmol) was added and the reaction stirred an additional 1 h at 0° C. Saturated sodium bicarbonate (500 mL) was added slowly and the suspension stirred 30 min and warmed to rt. The solution was extracted with EtOAc (3×400 mL), the combined organic layers washed with H2O (500 mL), saturated NaCl (500 mL), dried (Na2SO4), and concentrated in vacuo to give the title compound as a brown oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745484B2uspto-grants-2010_06