HuagongsheHuagongshe Chemistry Print Report · For research reference only
2',4'-Dihydroxyacetophenone → HCID 23110664, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2',4'-Dihydroxyacetophenone | HCID 6990 | — |
| Reactant | HCID 521026 | HCID 521026 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium hydroxide methanol | HCID 23689386 | — |
| Product | HCID 23110664 | HCID 23110664 | — |
Reaction Steps
2′,4′-Dihydroxyacetophenone (manufactured by Wako Pure Chemical Industries, Ltd.) was treated with 1-bromo-2-methyl-2-butene (manufactured by Aldrich) in 2 M KOH/methanol solution under ice-cooling, and thereafter the treated solution was hydrogenated in methanol, in the presence of palladium black (manufactured by Nakalai Tesque, Inc.), to give 2′,4′-dihydroxy-3′-(3-methylbutyl)acetophenone. Subsequently, 2′,4′-dihydroxy-3′-(3-methylbutyl)acetophenone and 4-hydroxybenzaldehyde (manufactured by Aldrich) were subjected to Claisen condensation, to give a yellow substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498357B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-01f836b342f54dd0904850f3d1fe6486 |
| Source note | uspto-grants-2009_03 |