Reacción #58039
ord-96b54c9a3c1a42999c07ec1e126ca2be
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ConcentraciónThe reaction mixture was concentrated under reduced pressure and methylene chloride (50 mL)
- 2workup.ADDITIONwas added to the residue
- 3OtroThe organic phase was dried
- 4Concentraciónconcentrated 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%).