Reacción #655181
ord-ccaca81eba15407fac63fc44cfd8354c
Ecuación de reacción
1,3-benzodioxole
n-butyllithium
NaHCO3
carbon dioxide
→
2,3-methylenedioxyphenylcarboxylic acid
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.ADDITIONWhen the addition
- 2Temperaturaunder reflux for one hour
- 3workup.ADDITIONit was added
- 4OtroThe alkali layer was separated
- 5Lavadowashed with ether
- 6Extracciónextracted with chloroform
- 7SecadoThe combined organic layers were dried over MgSO4
- 8Filtraciónfiltered
- 9Concentraciónconcentrated under reduced pressure (1.1 g, 20%)
Procedimiento
A solution of 1,3-benzodioxole (3.09 g, 32 mmol) in dry ether (50 mL) was treated dropwise at −10° C. with 2.5 M n-butyllithium (15 mL, 35 mmol) in hexane. When the addition was complete, the mixture was stirred under reflux for one hour. After cooling to room temperature, it was added to crushed solid carbon dioxide, and after 24 hours, the residue was treated with 10% aq. NaHCO3 and ether. The alkali layer was separated, washed with ether, then acidified with cold concentrated HCl, and extracted with chloroform. The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure (1.1 g, 20%). EI-MS m/z 167 (M+H)+.