HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5,7,3',4'-Pentahydroxyflavanone → Vanillin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5,7,3',4'-Pentahydroxyflavanone | HCID 471 | — |
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | HCID 54119736 | HCID 54119736 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Vanillin | HCID 1183 | 1% |
| Product | 2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol | HCID 1203 | — |
| Product | HCID 54119736 | HCID 54119736 | — |
Reaction Steps
Working solution of 1% vanillin was prepared by dissolving 0.1 g of vanillin in 10 mL of 5 N HCl, whereas 5% dimethylaminocinnamaldehyde (DMACA) was prepared in methanol containing 5% H2SO4. Lyophilized extract for 100 mg of dry kernels was dissolved in 0.5 mL of vanillin or DMACA working solutions. Taxifolin and catechin each at a concentration of 100 ppm were used as reference compounds for color reactions. Because vanillin is catechin-specific and produces bright red color, no color is developed when it reacts with taxifolin. DMACA reacting with catechin produces dark greenish blue color, whereas reacting with taxifolin produces purple color.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348475B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-1f667d9385214a6a8ee33448a7929562 |
| Source note | uspto-grants-2008_03 |