反応 #56479

反応方程式

acetonitrile

tetrahydrofuran

n-butyl lithium

diisopropylamine

tetrahydrofuran

hexanal

tetrahydrofuran

hydrochloric acid

→

title compound

収率 92.0%

1-Amino-3-(tetrahydro-2H-pyran-2-yloxy)octane

収率 92.0%

溶媒

hexane

反応条件

後処理

1. 1
   温度cooled to -78° C.
2. 2
   workup.STIRRINGThe resulting turbid suspension is stirred
3. 3
   温度maintained at -78° C. for 30 minutes
4. 4
   温度cooling at -78° C.
5. 5
   温度is maintained for an additional 15 minutes
6. 6
   抽出extracted with ether (100 ml.)
7. 7
   抽出The organic extract
8. 8
   洗浄is washed with water (50 ml.) and 5% aqueous sodium bicarbonate (50 ml.)
9. 9
   乾燥dried over magnesium sulfate
10. 10
    ろ過filtered
11. 11
    その他evaporated in vacuo

実験手順

A 1.9 M solution (21 ml. 40 millimole) of n-butyl lithium in hexane is added cautiously to a stirred solution of freshly distilled diisopropylamine (4.04 g., 40 millimole) in anhydrous tetrahydrofuran (60 ml.) maintained at 0° C. under a nitrogen atmosphere. The resulting solution is stirred at ambient temperature for 15 minutes, cooled to -78° C., and treated with a solution of anhydrous acetonitrile (1.64 g., 40 millimole) in anhydrous tetrahydrofuran (5 ml.). The resulting turbid suspension is stirred and maintained at -78° C. for 30 minutes and then treated with a solution of hexanal (4.0 g., 40 millimole) in anhydrous tetrahydrofuran (5 ml.). After attaining a clear, yellow reaction solution, cooling at -78° C. is maintained for an additional 15 minutes. The cold reaction solution is treated with 2 N hydrochloric acid (50 ml.) and extracted with ether (100 ml.). The organic extract is washed with water (50 ml.) and 5% aqueous sodium bicarbonate (50 ml.), dried over magnesium sulfate, filtered and evaporated in vacuo, leaving the title compound as a pale yellow oil (5.2 g., 92%), pmr (CDCl3) δ0.97 (3H, t), 2.55 (2H, d), 3.10 (H, s) and 3.93 (H, bs).

出典