Реакция #362621

ord-912ed703e1954c0a984471dd243a718c

Реагенты

Нет

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураto cool
  2. 2
    Другоеreached about 40° C.
  3. 3
    Температураto cool to room temperature
  4. 4
    ЭкстракцияThe reaction mixture was extracted twice with 100 ml ethyl ether
  5. 5
    Промывкаwashed with 200 ml of 1.5M aqueous sodium carbonate
  6. 6
    ДругоеThe aqueous layer was separated
  7. 7
    workup.ADDITIONby adding concentrated HCl
  8. 8
    ЭкстракцияThe acidified aqueous layer was extracted with 200 ml ethyl ether
  9. 9
    ДругоеThe organic layer was separated
  10. 10
    Сушкаdried with MgSO4
  11. 11
    Фильтрацияfiltered
  12. 12
    ДругоеThe solvent was removed in vacuo

Методика

To a solution of m-fluorophenol (24.2 g, 0.22 mol) in 79.2 ml of 25% aqueous sodium hydroxide heated to 45° C. with an oil bath was added 29.5 ml (0.26 mol) methyl 2-chloropropionate. The reaction mixture was heated to 80° C. for 17 hours and then allowed to cool. When the temperature reached about 40° C., concentrated HCl (25 ml) was added and the reaction mixture was allowed to cool to room temperature. The reaction mixture was extracted twice with 100 ml ethyl ether. The organic layers were combined and washed with 200 ml of 1.5M aqueous sodium carbonate. The aqueous layer was separated and acidified to pH 1, by pH test paper, by adding concentrated HCl. The acidified aqueous layer was extracted with 200 ml ethyl ether. The organic layer was separated, dried with MgSO4 and filtered. The solvent was removed in vacuo to yield 17 g (41% yield) of 2-(3' -fluorophenoxy)propionic acid as a yellow solid (m.p. 72.5°-74° C.).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05393735uspto-grants-1995_02