반응 #411885
ord-bb2021ce32a34a9d83b9e17c7efcd92c
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용매
반응 조건
후처리
- 1온도was refluxed for 3 h
- 2온도the reaction was heated
- 3온도to reflux for an additional 3.5 h
- 4온도cooled
- 5여과filtered through a pad of celite
- 6세척eluting with 0.5-4% CH3OH/CH2Cl2
- 7workup.ADDITIONThe fractions containing product
- 8세척washed successively with sat aq NaHCO3 10% Na2S2O3, and brine
- 9건조dried (MgSO4)
- 10농축concentrated in vacuo
실험 절차
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).