反应 #481603

ord-b4f371c21ea54f5c89ca51bdd0bd6a04

反应方程式

[Na+].[OH-]
Sodium hydroxide
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenyl phosphine
CCOC(=O)C(C)Br
ethyl-2-bromopropionate
c1ccccc1
benzene
O=C1OC(c2ccc(O)cc2)(c2ccc(O)cc2)c2ccccc21
phenolphthalein
C[PH2]=CC(=O)OCC(c1ccccc1)(c1ccccc1)c1ccccc1
triphenyl methyl carbethoxy methylene phosphorane

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他at room temperature
  2. 2
    萃取Extraction with benzene, concentration of the benzene
  3. 3
    萃取extract
  4. 4
    workup.ADDITIONthe addition of petroleum ether (60-80° C.)

实验过程

Monodemethylation of 3,4,5-trimethoxy benzaldehyde using sulphuric acid at 40° C. for 8 hours as described above in Example 1 yields syringaldehyde. The Wittig salt is prepared by reaction of triphenyl phosphine and ethyl-2-bromopropionate in benzene media at 70-75 ° C. for 8 hours and subsequent basification with 1N Sodium hydroxide to phenolphthalein end point at room temperature. Extraction with benzene, concentration of the benzene extract and the addition of petroleum ether (60-80° C.) yield triphenyl methyl carbethoxy methylene phosphorane as a solid product. Condensation of 3,5-Dimethoxy-4-hydroxy benzaldehyde (Syringaldehyde) with triphenyl methyl carbethoxy methylene phosphorane is performed at reflux temperature in xylene for seven hours and after work up, yields the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06602515B2uspto-grants-2003_08