Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Cyclododecane | HCID 9268 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Cyclododecanone | HCID 13246 | 7.3% |
| Product | Cyclododecanol | HCID 15595 | 13.1% |
Reaction Steps
In a flask having an internal volume of 100 ml, 8.4 g (50 mmol) of cyclododecane, 4.52 g of acetic acid, 16.3 mg (0.1 mmol) of N-hydroxyphthalimide, 28.9 mg (0.1 mmol) of bis(acetylacetonato)manganese(II) dihydrate, and 2.0 mg (0.01 mmol) of cobalt(II) acetate tetrahydrate were placed, and an oxygen balloon was attached to the reactor. The liquid temperature was raised on an oil bath and was held at 100° C. The reaction was terminated by cooling 6 hours later. A reaction mixture was diluted with 60 g of acetic acid to thereby dissolve all of solid matters. The resulting solution was analyzed to find that a conversion from cyclododecane was 20.6% and a selectivity for dodecanedioic acid was 23.7%. In addition, cyclododecanone (selectivity: 7.3%) and cyclododecanol (selectivity: 13.1%) were by-produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07015356B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-cb86508fbfa6497bba763938d464c601 |
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| Source note | uspto-grants-2006_03 |
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