Реакция #411885
ord-bb2021ce32a34a9d83b9e17c7efcd92c
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураwas refluxed for 3 h
- 2Температураthe reaction was heated
- 3Температураto reflux for an additional 3.5 h
- 4Температураcooled
- 5Фильтрацияfiltered through a pad of celite
- 6Промывкаeluting with 0.5-4% CH3OH/CH2Cl2
- 7workup.ADDITIONThe fractions containing product
- 8Промывкаwashed successively with sat aq NaHCO3 10% Na2S2O3, and brine
- 9Сушкаdried (MgSO4)
- 10Концентрированиеconcentrated 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).