Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Oleic Acid | HCID 445639 | — |
| Reactant | Linoleic Acid | HCID 5280450 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Product | Azelaic Acid | HCID 2266 | 70.9% |
| Product | Nonanoic Acid | HCID 8158 | 70% |
Reaction Steps
Into a 500 ml round bottomed flask equipped with a mechanical stirrer, thermometer, dropping funnel, gas influx tube and a condenser, 100 g of crude oleic acid (80% purity) containing 9% linoleic acid and 0.75 g of H2WO4 is added. The stirred mixture is brought to 60°-65° C. and 28 g of 60% w/w H2O2 is added. The H2O2 is gradually added over about 30 mins in order to maintain the temperature between 65°-75° C. Once the addition of H2O2 is completed the mixture is left at that temperature for 1.5 hours. Then, 200 ml of water and 1 g of hydrous cobalt acetate is added to the mixture. The temperature is raised to 70° C. by passing an oxygen stream through the reactor bottom for 4 hours. At the end of the reaction, the reaction products are recovered by the process as described in example 1, obtaining 42.5 g of azelaic acid (yield=70.9%) and 31.3 g of pelargonic acid (yield=70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05714623 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-28db4b605d4f49c9be6cc669c688945b |
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| Source note | uspto-grants-1998_02 |
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