تفاعل #3778

ord-b4abd6c40e154847ac62183456b57efd

معادلة التفاعل

CCCCCO
Amyl alcohol
COc1cccc(O)c1OC
2,3-dimethoxyphenol
CC(=O)c1ccccc1Br
2'-bromoacetophenone
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1cccc(OCC(=O)c2ccccc2)c1OC
2-(2,3-dimethoxyphenoxy)acetophenone
المردود 87.0%

المذيبات

ظروف التفاعل

درجة الحرارة
150°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةby heating
  2. 2
    غسيلthe resulting solution was washed in dilute hydrochloric acid, in water
  3. 3
    تجفيفin a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONthe solvents therein were distilled off under reduced pressure
  5. 5
    أخرىThe residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=8:1)

الإجراء التجريبي

Amyl alcohol (44 ml) was added to 2,3-dimethoxyphenol (5 g), 2'-bromoacetophenone (7 g), potassium carbonate (6.7 g) and copper acetate (1.1 g), followed by heating and stirring at 150° C. for 8 hours for reacting them together. To the reaction solution was added ethyl acetate (300 ml), and the resulting solution was washed in dilute hydrochloric acid, in water, and in a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvents therein were distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=8:1), to recover 2-(2,3-dimethoxyphenoxy)acetophenone (7.6 g; yield of 87%). By 1H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05734067uspto-grants-1998_03