Реакция #411885

ord-bb2021ce32a34a9d83b9e17c7efcd92c

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas refluxed for 3 h
  2. 2
    Температураthe reaction was heated
  3. 3
    Температураto reflux for an additional 3.5 h
  4. 4
    Температураcooled
  5. 5
    Фильтрацияfiltered through a pad of celite
  6. 6
    Промывкаeluting with 0.5-4% CH3OH/CH2Cl2
  7. 7
    workup.ADDITIONThe fractions containing product
  8. 8
    Промывкаwashed successively with sat aq NaHCO3 10% Na2S2O3, and brine
  9. 9
    Сушкаdried (MgSO4)
  10. 10
    Концентрированиеconcentrated in vacuo

Методика

A suspension of 2-chloro-4-pyridinemethanol (8.0 g, 55.9 mmol), NBS (14.9 g, 83.9 mmol), and K2CO3 (11.75 g, 97.1 mmol) in EtOAc was refluxed for 3 h. A second portion of NBS (14.9 g, 83.9 mmol) and Na2CO3 (12.0 g, 114 mmol) were added and the reaction was heated to reflux for an additional 3.5 h, cooled and filtered through a pad of celite. The filtrate, after concentrattion to a small volume, was subjected to flash chromatography eluting with 0.5-4% CH3OH/CH2Cl2. The fractions containing product were combined, washed successively with sat aq NaHCO3 10% Na2S2O3, and brine, dried (MgSO4) and concentrated in vacuo to give the title compound as a light yellow solid; yield 5.3 g (67%). 1H NMR (CDCl3) δ10.06 (s, 1H), 8.66 (d, 1H, J=5.0 Hz), 7.76 (s, 1H), 7.66 (d, 1H, J=5.0 Hz).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06218537B1uspto-grants-2001_04