反应 #1244247

ord-d5eca52ef81147d8b22377cb6ac8bcbf

反应方程式

CCC(=O)Cl
propanoyl chloride
Oc1ccc(N=Nc2ccccc2)cc1
4-Phenylazophenol
CCN(CC)CC
triethylamine
CCC(=O)Oc1ccc(N=Nc2ccccc2)cc1
product
收率 72.0%
CCC(=O)Oc1ccc(N=Nc2ccccc2)cc1
Propionic acid 4-phenylazo-phenyl ester
收率 72.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他reaction
  2. 2
    洗涤The reaction mixture was washed with water
  3. 3
    workup.ADDITIONdilute acid and brine
  4. 4
    干燥dried with magnesium sulfate
  5. 5
    其他The solvent was evaporated

实验过程

4-Phenylazophenol (0.25 g, 1.26 mmoles) was dissolved in ether (5-10 mL) and triethylamine (0.26 mL) was added. Then propanoyl chloride (0.14 g 1.5 mmoles) in ether (1 mL) was added dropwise at room temperature. The mixture was stirred and reaction was rapidly completed. The reaction mixture was washed with water, dilute acid and brine and dried with magnesium sulfate. The solvent was evaporated to give 0.23 g (72%) of product. 1H NMR (CDCl3) δ=1.16 (3H, t, J=7.7), 2.40 (2H, q J=7.7), 7.25 (2H, m), 7.40-7.58 (3H, m), 7.88-8.0 (4H, m) ppm.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07807075B2uspto-grants-2010_10