Reacción #58039

ord-96b54c9a3c1a42999c07ec1e126ca2be

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction mixture was concentrated under reduced pressure and methylene chloride (50 mL)
  2. 2
    workup.ADDITIONwas added to the residue
  3. 3
    OtroThe organic phase was dried
  4. 4
    Concentraciónconcentrated under reduced pressure

Procedimiento

A solution of trans-[4-(benzylimino-methyl)-cyclohexyl]-carbamic acid tert-butyl ester (2.50 g, 8.00 mmol) and oxalic acid (0.80 g) in water/THF (50 mL, 1:1) was stirred for 10 h at room temperature. The reaction mixture was concentrated under reduced pressure and methylene chloride (50 mL) was added to the residue. The organic phase was dried and concentrated under reduced pressure to give trans-(4-Formyl-cyclohexyl)-carbamic acid tert-butyl ester (1.3 g, 80%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07423012B2uspto-grants-2008_09