Hydrochloric Acid → 2-(6-Chloropyridin-2-yl)ethanol
反応式
C([O:3][C:4](=O)[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Cl:12])[N:7]=1)C.[Li+].[BH4-].O.Cl>C1COCC1>[Cl:12][C:8]1[N:7]=[C:6]([CH2:5][CH2:4][OH:3])[CH:11]=[CH:10][CH:9]=1C([O:3][C:4](=O)[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Cl:12])[N:7]=1)C.[Li+].[BH4-].O.Cl>C1COCC1>[Cl:12][C:8]1[N:7]=[C:6]([CH2:5][CH2:4][OH:3])[CH:11]=[CH:10][CH:9]=1To a solution of ethyl(6-chloro-2-pyridinyl)acetate (Example 469, 5.00 g, 25 mmol) in THF (50 mL) was added LiBH4 (13.0 mL, 25.0 mmol, 2M solution in THF) at 0° C. The mixture was stirred at rt for 18 h, then water was slowly added [strong gaseous evolution] followed by HCl (10 mL, 1N aqueous solution). The mixture was extracted with CH2Cl2. The combined organic phases were dried (Na2SO4), filtered and then concentrated under reduced pressure. The residue was purified using a short pad of silica gel (4:1 hexanes/EtOAc) to give the product (3.00 g, 76%) as a light-yellow oil which solidified upon standing. 1H NMR (400 MHz, CDCl3) δ 2.97 (t, 2H), 3.98 (t, 2H), 7.10 (dd, 2H), 7.54 (t, 1H).
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