Reacción #43295

ord-7ab66d16e9c8458ca22df66b17239717

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturarefluxed for 20 hours
  2. 2
    Filtraciónfiltered hot
  3. 3
    Otrothe filtrate was evaporated
  4. 4
    OtroThe residue was purified by column chromatography over silica gel (eluent: DCM)
  5. 5
    OtroThe desired fractions were collected
  6. 6
    Otrothe solvent was evaporated
  7. 7
    workup.ADDITIONToluene was added
  8. 8
    Otroazeotroped on the rotary evaporator

Procedimiento

A mixture of 5-chloro-2,3-dihydroxy-benzoic acid methyl ester (0.3 mol), 1,3-dibromopropane (0.42 mol) and K2CO3 (0.66 mol) in 2-propanone (500 ml) was stirred and refluxed for 20 hours, then filtered hot and the filtrate was evaporated. The residue was purified by column chromatography over silica gel (eluent: DCM). The desired fractions were collected and the solvent was evaporated. Toluene was added and azeotroped on the rotary evaporator, yielding 69 g of methyl 8-chloro-3,4-dihydro-2H-1,5-benzodioxepin-6-carboxylate (intermediate 5).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732464B2uspto-grants-2010_06