Reaktion #362621

ord-912ed703e1954c0a984471dd243a718c

Reaktionsgleichung

Oc1cccc(F)c1
m-fluorophenol
COC(=O)C(C)Cl
methyl 2-chloropropionate
Cl
HCl
CC(Oc1cccc(F)c1)C(=O)O
2-(3' -fluorophenoxy)propionic acid
Ausbeute 42.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto cool
  2. 2
    Sonstigereached about 40° C.
  3. 3
    Temperaturto cool to room temperature
  4. 4
    ExtraktionThe reaction mixture was extracted twice with 100 ml ethyl ether
  5. 5
    Waschenwashed with 200 ml of 1.5M aqueous sodium carbonate
  6. 6
    SonstigeThe aqueous layer was separated
  7. 7
    workup.ADDITIONby adding concentrated HCl
  8. 8
    ExtraktionThe acidified aqueous layer was extracted with 200 ml ethyl ether
  9. 9
    SonstigeThe organic layer was separated
  10. 10
    Trocknendried with MgSO4
  11. 11
    Filtrationfiltered
  12. 12
    SonstigeThe solvent was removed in vacuo

Vorschrift

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.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05393735uspto-grants-1995_02