Реакция #82227

ord-2031b461fb474e2485dbe138cd102dc3

Уравнение реакции

CC(=O)c1cc(Br)ccc1O
2-acetyl-4-bromophenol
CCOC(=O)CBr
ethyl bromoacetate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOC(=O)COc1ccc(Br)cc1C(C)=O
ethyl (2-acetyl-4-bromophenyl)oxyacetate
Выход 90.2%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеInsoluble materials were removed by filtration
  2. 2
    Концентрированиеthe resulting filtrate was concentrated
  3. 3
    Другоеdried
  4. 4
    ДругоеThe residue thus obtained
  5. 5
    Промывкаwashed with water
  6. 6
    Другоеdried
  7. 7
    Другоеto remove the solvent
  8. 8
    ПромывкаThe thus treated residue was washed with a mixed solvent system of ethanol and n-hexane
  9. 9
    Другоеto isolate insoluble crystals
  10. 10
    Фильтрацияby filtration

Методика

13.31 g of 2-acetyl-4-bromophenol, 11.0 g of ethyl bromoacetate and 9.7 g of anhydrous potassium carbonate were refluxed under heating in 70 ml of acetone for 2 hours. Insoluble materials were removed by filtration, and the resulting filtrate was concentrated and dried. The residue thus obtained was dissolved in chloroform, washed with water, and then dried to remove the solvent. The thus treated residue was washed with a mixed solvent system of ethanol and n-hexane to isolate insoluble crystals by filtration. In this way, 16.82 g of ethyl (2-acetyl-4-bromophenyl)oxyacetate was obtained in the form of colorless plate crystals.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05620991uspto-grants-1997_04