HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20254624, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 6-(11-Hydroxy-1-oxoundecyl)-2,3-dimethoxy-5-methylphenol | HCID 13276236 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 20254624 | HCID 20254624 | — |
Reaction Steps
To a solution of 6-(11-hydroxy-1-oxoundecyl)-2,3-dimethoxy-5-methylphenol (14 g) in acetic acid (200 ml) are added 5% palladium-on-carbon (50% hydrous) (3 g) and 70% perchloric acid (0.1 ml), and catalytic reduction is carried out at atmospheric temperature and pressure. When the hydrogen has ceased to be absorbed, the catalyst is filtered off and the filtrate is concentrated under reduced pressure. The residue is extracted with dichloromethane and the dichloromethane layer is washed with a 5% aqueous solution of sodium hydrogen carbonate and dried over anhydrous magnesium sulfate. The solvent is then distilled off to obtain a colorless oil of 6-(11-acetoxyundecyl)-2,3-dimethoxy-5-methylphenol (15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04495104 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-d2e8c95e4ee44144a89b5834af3bb39c |
| Source note | uspto-grants-1985_01 |