Reacción #699841

ord-95cf0bf151df4e3eb9d5d17775e3edbf

Ecuación de reacción

c1ccc2c(c1)OCO2
1,3-benzodioxole
[Li][CH2]CCC
n-butyllithium
O=C([O-])O.[Na+]
NaHCO3
O=C=O
carbon dioxide
O=C(O)c1cccc2c1OCO2
2,3-methylenedioxyphenylcarboxylic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONWhen the addition
  2. 2
    Temperaturaunder reflux for one hour
  3. 3
    workup.ADDITIONit was added
  4. 4
    OtroThe alkali layer was separated
  5. 5
    Lavadowashed with ether
  6. 6
    Extracciónextracted with chloroform
  7. 7
    SecadoThe combined organic layers were dried over MgSO4
  8. 8
    Filtraciónfiltered
  9. 9
    Concentraciónconcentrated 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 2.5M 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)+

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06005008uspto-grants-1999_12