Reacción #350558

ord-743792ceed5c4c4ea3c47955251be809

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe organic phase was separated
  2. 2
    Secadodried (MgSO4)
  3. 3
    Otroevaporated

Procedimiento

Thionylchloride (44 ml) was added dropwise with water-cooling to a solution of 5-chloro-3-(4-fluorophenyl)-2,3-dihydro-1H-inden-1-ol in ether (2L) with a catalytic amount of DMF (0.5 ml). Then the mixture was stirred for 2 hours at room temperature, poured into ice and neutralized with 9N NaOH. The organic phase was separated, dried (MgSO4) and evaporated to give 140 g of crude 1,5-dichloro-3-(4-fluorophenyl)-2,3-dihydro-1H-inden.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05643784uspto-grants-1997_07