Reaktion #362621
ord-912ed703e1954c0a984471dd243a718c
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturto cool
- 2Sonstigereached about 40° C.
- 3Temperaturto cool to room temperature
- 4ExtraktionThe reaction mixture was extracted twice with 100 ml ethyl ether
- 5Waschenwashed with 200 ml of 1.5M aqueous sodium carbonate
- 6SonstigeThe aqueous layer was separated
- 7workup.ADDITIONby adding concentrated HCl
- 8ExtraktionThe acidified aqueous layer was extracted with 200 ml ethyl ether
- 9SonstigeThe organic layer was separated
- 10Trocknendried with MgSO4
- 11Filtrationfiltered
- 12SonstigeThe 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.).