반응 #1244247

ord-d5eca52ef81147d8b22377cb6ac8bcbf

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타reaction
  2. 2
    세척The reaction mixture was washed with water
  3. 3
    workup.ADDITIONdilute acid and brine
  4. 4
    건조dried with magnesium sulfate
  5. 5
    기타The solvent was evaporated

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07807075B2uspto-grants-2010_10