HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclododecanone → 13-Oxabicyclo[10.1.0]tridecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclododecanone | HCID 13246 | — |
| Reactant | Cyclododecanol | HCID 15595 | — |
| Product | 13-Oxabicyclo[10.1.0]tridecane | HCID 9248 | — |
Reaction Steps
After the reaction was completed, the catalyst was removed from the reaction product mixture by filtering, and the reaction product mixture was subjected to gas chromatographic analysis. As a result, it was found that cyclododecanol was obtained in a yield of 6 molar % based on the fed epoxycyclododecadiene, and cyclododecanone was obtained in a yield of 76 molar %. Thus, the total yield of cyclododecanol and cyclododecanone was 82 molar %. In the reaction, epoxycyclododecane was produced in a yield of 16 molar %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06335472B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-3669fd70b92b47e5b249bda2f2d404ff |
| Source note | uspto-grants-2002_01 |