Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Oleic Acid | HCID 445639 | — |
| Reactant | Linoleic Acid | HCID 5280450 | — |
| Catalyst | Cobalt(II) chloride | HCID 24288 | — |
| Product | Azelaic Acid | HCID 2266 | 70% |
| Product | Nonanoic Acid | HCID 8158 | 69% |
Reaction Steps
Using the same apparatus as in Example 1, 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. The crude reaction product so obtained is charged into an stirred 500 ml autoclave containing 150 ml of water and 1.0 g of hydrous cobalt chloride. The autoclave is then pressurised with 65 atm of air and the temperature is raised to 70° C. The reaction mixture is treated according to the way described in example 1 obtaining 42 g of azelaic acid (yield=70%) and 30.9 g of pelargonic acid (yield=69%).
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-abb9eac2712f41f7bad0a8b5acc023cc |
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| Source note | uspto-grants-1998_02 |
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