Реакция #831100

ord-4e0743878087423c9cb1b41bf7471d5d

Уравнение реакции

O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)(C)OC(=O)CBr
tert-butyl bromoacetate
C=Cc1ccc(O)cc1
4-hydroxystyrene
CC(C)=O
acetone
C=Cc1ccc(OCC(=O)OC(C)(C)C)cc1
desired product
Выход 98.5%
C=Cc1ccc(OCC(=O)OC(C)(C)C)cc1
tert-butyl 4-vinylphenoxyacetate
Выход 98.5%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooled
  2. 2
    Фильтрацияfiltered
  3. 3
    Другоеevaporated
  4. 4
    ДругоеThe residue obtained
  5. 5
    Промывкаwashed twice with 100 ml of 1N NaOH solution in each case
  6. 6
    ДругоеThe organic phase is separated off
  7. 7
    Сушкаdried over magnesium sulfate
  8. 8
    Другоеevaporated

Методика

59.3 g (430 mmol) of potassium carbonate, 0.64 g of potassium iodide, 50.7 g (260 mmol) of tert-butyl bromoacetate and 31.2 g (260 mmol) of 4-hydroxystyrene are mixed with 145 ml of acetone in a 750 ml sulfonation flask. The resultant suspension is refluxed for 100 minutes, cooled, filtered and evaporated. The residue obtained is taken up in 750 ml of ether and washed twice with 100 ml of 1N NaOH solution in each case and then twice with 200 ml of water in each case. The organic phase is separated off, dried over magnesium sulfate and evaporated, leaving 60.02 g (256 mmol) of the desired product as a clear oil, which corresponds to a yield of 98.5% of theory. 1H-NMR (CDCl3, 300 MHz): δ ppm] 7.33/d/2H of the resultant product 6,84/d/2H 6,64/dd/1H 5,60/d/1H 5,12/d/1H 4,49/s/2H 1,47/s/9H

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05558978uspto-grants-1996_09