反応 #1452754

ord-bc3d4a13cbc1409f9737559de30badd6

反応方程式

O
water
O=C([O-])[O-].[K+].[K+]
Potassium carbonate
O=[N+]([O-])c1ccc(O)cc1
4-nitrophenol
COCCOCCOCCOS(=O)(=O)c1ccc(C)cc1
13
COCCOCCOCCOS(=O)(=O)c1ccc(C)cc1
2-[2-(2-methoxyethoxy)ethoxy]ethyl p-toluenesulfonate
COCCOCCOCCc1ccc([N+](=O)[O-])cc1
product
収率 77.1%
COCCOCCOCCc1ccc([N+](=O)[O-])cc1
4-{2-[2-(2-methoxyethoxy)ethoxy]ethyl}nitrobenzene
収率 77.1%

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度After cooling to room temperature
  2. 2
    抽出extracted three times with methylene chloride
  3. 3
    洗浄The combined organic layers were washed with water
  4. 4
    乾燥brine, dried over magnesium sulfate
  5. 5
    ろ過filtered
  6. 6
    その他the solvent was removed by distillation at reduced pressure

実験手順

A portion of 13 (9.0 g, 28.3 mmol) was dissolved in 50 mL of dimethylformamide. Potassium carbonate (11.75 g, 85.0 mmol) and 4-nitrophenol (3.82 g, 27.5 mmol) were added. The solution was stirred at 80° C. for 16 hours. After cooling to room temperature, the solution was poured into water and extracted three times with methylene chloride. The combined organic layers were washed with water, then brine, dried over magnesium sulfate, filtered, and the solvent was removed by distillation at reduced pressure. Chromatography (silica, hexane:ethyl acetate, 1:2) was employed to isolate the product (5.71 g, 73% yield). IR (neat) 3109.2, 3078.2, 2878.5, 1726.3, 1588.1, 1511.2, 1337.1, 1106.7, 1050.3, 932.6, 845.5, 753.3, 656.1 cm−1.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07892517B2uspto-grants-2011_02