反应 #502077

ord-96543556ab9b474d9c1a8f42a558083f

反应方程式

CC(C)CCCC(C)O
6-methylheptan-2-ol
[H-].[Na+]
Sodium hydride
CN(C)C=O
dimethylformamide
CC(C)CCCC(C)OCCCCC1OCCO1
2-{4-[(1,5-dimethylhexyl) oxy]butyl}-1,3-dioxolane
收率 19.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他fitted with thermocouple, magnetic stirrer, condenser
  2. 2
    萃取extracted with methyltert-butyl ether (2×100 mL)
  3. 3
    干燥the combined organic phase dried over magnesium sulphate
  4. 4
    其他the solvent removed in vacuo
  5. 5
    其他The pale yellow oil was chromatographed over silica gel

实验过程

Sodium hydride (60% dispersion in mineral oil, 0.83 g, 20 mmol) and dimethylformamide (70 mL) were charged to a 250 mL three necked flask fitted with thermocouple, magnetic stirrer, condenser and dropping funnel. To the reaction mixture was added dropwise over 10 minutes 6-methylheptan-2-ol (2.77 g, 21 mmol). The reaction mixture was stirred at room temperature for 90 minutes then water (10 mL) was added. The reaction mixture was poured into water (100 mL), extracted with methyltert-butyl ether (2×100 mL), the combined organic phase dried over magnesium sulphate and the solvent removed in vacuo. The pale yellow oil was chromatographed over silica gel to yield 2-{4-[(1,5-dimethylhexyl) oxy]butyl}-1,3-dioxolane as a colourless oil (1.4 g, 73% pure by GC RPA, 3.9 mmol, chemical yield 19%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08088725B2uspto-grants-2012_01