تفاعل #1153143

ord-950eaab79849496da2cb9d7fe7039fdb

معادلة التفاعل

COc1cc(O)c(C=O)c(OC)c1
4,6-dimethoxy-2-hydroxybenzaldehyde
COc1ccc(C(C)=O)cc1
4-methoxyacetophenone
Cl
HCl
Oc1ccc(-c2ccc3c(O)cc(O)cc3[o+]2)cc1.[Cl-].[Cl-]
apigenidin chloride

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto obtain
  2. 2
    ترشيحafter filtration

الإجراء التجريبي

One method consists, for example, in preparing, in a first step, trimethylapigenidin by condensation of commercially available 4,6-dimethoxy-2-hydroxybenzaldehyde with commercially available 4-methoxyacetophenone at 0° C. in anhydrous ether medium, and saturation with anhydrous HCl in order to obtain, after filtration, an orange-red precipitate of trimethylapigenidin. In a second step, in hydrolysing the trimethylapigenidin obtained in the preceding step to apigenidin chloride, the reaction being carried out in an HI and phenol and AgCl medium in solution in methanol. Such a method of synthesis is described by R. Robinson and A. Robertson in J., Chem., Soc. 1951-(1926) and 2196-(1927).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06241785B1uspto-grants-2001_06