Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Cyclododecane | HCID 9268 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Cyclododecanone, oxime | HCID 136762 | — |
| Reactant | Nitrocyclododecane | HCID 292842 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Cyclododecanone | HCID 13246 | — |
Reaction Steps
Cyclododecane (3.32 g; 19.8 mmol), N-hydroxyphthalimide (0.8 mmol), and acetic acid (4 ml) were placed in a flask, t-butyl nitrite (4 mmol) was added to the mixture in four installments of 1 mmol each once every 30 minutes with stirring at 70° C. in an atmosphere of argon gas for a total of 2.5 hours. The mixture was further treated with sulfuric acid having a concentration of 98% by weight (200 mg) with stirring at 70° C. for 15 minutes, was neutralized with sodium hydroxide and was analyzed to find that cyclododecanone oxime, nitrocyclododecane, and cyclododecanone were formed in yields of 65%, 2%, and 5%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06768023B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-2e5f791578b840a68a657cd17b4bb5f6 |
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| Source note | uspto-grants-2004_07 |
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