Reacción #362621
ord-912ed703e1954c0a984471dd243a718c
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturato cool
- 2Otroreached about 40° C.
- 3Temperaturato cool to room temperature
- 4ExtracciónThe reaction mixture was extracted twice with 100 ml ethyl ether
- 5Lavadowashed with 200 ml of 1.5M aqueous sodium carbonate
- 6OtroThe aqueous layer was separated
- 7workup.ADDITIONby adding concentrated HCl
- 8ExtracciónThe acidified aqueous layer was extracted with 200 ml ethyl ether
- 9OtroThe organic layer was separated
- 10Secadodried with MgSO4
- 11Filtraciónfiltered
- 12OtroThe solvent was removed in vacuo
Procedimiento
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.).