반응 #481606

ord-a1c677779ef440ee8fe0368662d58c1d

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타at 40° C.
  2. 2
    기타for 8 hours

실험 절차

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%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06602515B2uspto-grants-2003_08