HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Dehydroabietic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Abietic Acid | HCID 10569 | — |
| Reactant | Hydroxypropylene | HCID 143500 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Dehydroabietic Acid | HCID 94391 | — |
Reaction Steps
said abietic acid at 200–300° C. for 1–5 hours with the catalyst of 0.1–5% (wt) of 5%–10% palladium/carbon, or incubating directly at 220–380° C. After incubation and cooling down, adding 0.5 to 10-fold (volume) solvent, said solvent can be any one of methanol, ethanol, propenol, acetyester acetic acid, benzene and methbenzene, keeping refluxed for 1–3 hours, filtering when it is warm, cooling down, allowing it to stand for overnight and be crystallized. Dehydroabietic acid is obtained after filtering.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015343B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-a674de46ce834a52b48eb19e4e6e755e |
| Source note | uspto-grants-2006_03 |