反応 #1687620

反応方程式

2

3-Cyano-1-methylpyridinium Iodide

sodium borohydride

→

3Cyano-1-methyl-1,2,5,6-tetrahydropyridine

溶媒

methanol

water

反応条件

後処理

1. 1
   workup.ADDITIONAfter the addition the mixture
2. 2
   workup.DISTILLATIONMost of the methanol was distilled off
3. 3
   workup.ADDITIONTo the residue was added saturated ammonium chloride solution (200 ml)
4. 4
   抽出the mixture was extracted three times with ether (300 ml)
5. 5
   洗浄The combined organ phases wee washed once with water
6. 6
   抽出were then extracted three times with 4M hydrochloric
7. 7
   workup.WAITThe colored aqueous phases were kept for 1 hour at room temperature
8. 8
   抽出The mixture was extracted three times with ether (250 ml)
9. 9
   その他the combined organic phases were separated from the solid byproducts
10. 10
    洗浄The organic phase was washed with 4 portions of saturated sodium chloride solution (200 ml)
11. 11
    乾燥dried over magnesium sulphate
12. 12
    その他evaporated

実験手順

To a solution of 2 (133 g, 0.54 mol) in methanol (1000 ml) and water (200 ml) was added sodium borohydride (41 g, 1.08 mol) in portions at temperatures below 28° C. After the addition the mixture was stirred for 1 hour at room temperature. Most of the methanol was distilled off. To the residue was added saturated ammonium chloride solution (200 ml), and the mixture was extracted three times with ether (300 ml). The combined organ phases wee washed once with water and were then extracted three times with 4M hydrochloric and (300 ml). The colored aqueous phases were kept for 1 hour at room temperature, and pH was then adjusted to 14. The mixture was extracted three times with ether (250 ml), and the combined organic phases were separated from the solid byproducts. The organic phase was washed with 4 portions of saturated sodium chloride solution (200 ml), dried over magnesium sulphate and evaporated. This yielded 17.4 g (0.143 mol, 26%) of crude oily title compound, which was sufficiently pure according to the 1H NMR spectrum.

出典