HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20573874, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4'-Methoxyacetophenone | HCID 7476 | — |
| Reactant | 4,6-Dimethoxysalicylaldehyde | HCID 69725 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20573874 | HCID 20573874 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06241785B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-950eaab79849496da2cb9d7fe7039fdb |
| Source note | uspto-grants-2001_06 |