HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → Licochalcone A
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | 2-Methoxy-4-[(3-methyl-2-buten-1-yl)oxy]benzaldehyde | HCID 11085319 | — |
| Reactant | HCID 12153345 | HCID 12153345 | — |
| Product | Licochalcone A | HCID 5318998 | — |
Reaction Steps
The Claisen rearrangement of 2-methoxy-4-(3-methylbut-2-enyloxy)benzaldehyde and the Claisen condensation of the resulting 2-methoxy-4-hydroxy-5-(1,1-dimethyl-prop-2-enyl)benzaldehyde with 4-hydroxybenzaldehyde to give licochalcone A was performed according to the Chinese procedure:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06603046B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-d16904f34e714591989e32f92309d3f8 |
| Source note | uspto-grants-2003_08 |