تفاعل #1244247

ord-d5eca52ef81147d8b22377cb6ac8bcbf

معادلة التفاعل

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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىreaction
  2. 2
    غسيلThe reaction mixture was washed with water
  3. 3
    workup.ADDITIONdilute acid and brine
  4. 4
    تجفيفdried with magnesium sulfate
  5. 5
    أخرىThe solvent was evaporated

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07807075B2uspto-grants-2010_10