Reacción #481606

ord-a1c677779ef440ee8fe0368662d58c1d

Ecuación de reacción

COc1cc(C=O)cc(OC)c1OC
3,4,5-trimethoxy benzaldehyde
O=S(=O)(O)O
sulphuric acid
COc1cc(C=O)cc(OC)c1O
syringaldehyde

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat 40° C.
  2. 2
    Otrofor 8 hours

Procedimiento

Monodemethylation of 3,4,5-trimethoxy benzaldehyde using sulphuric acid at 40° C. for 8 hours as described above in Example 1 yields syringaldehyde. Transesterfication of diethyl malonate using 2-ethylhexyl alcohol in neat condition at 140-155° C. for 2 hours under nitrogen blanketing in the presence of sulphuric acid and after work up, followed by high vacuum distillation, yields di-6-ethylhexyl malonate. Condensation of 3,5-Dimethoxy-4-hydroxy benzaldehyde (Syringaldehyde) with di-2-ethylhexyl malonate in the presence of piperidine—acetic acid and benzene as the reaction medium at reflux temperature under continuous azeotropic water removal yields di-2-ethylhexyl-3,5-dimethoxy-4-hydroxy benzylidene malonate. The reaction takes about nine hours for completion. The yield typically obtained is 91%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06602515B2uspto-grants-2003_08