HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228882Generated: October 30, 2026
13-Oxabicyclo[10.1.0]tridecane → Cyclododecanone
https://huagongshe.com/reaction/2228882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 13-Oxabicyclo[10.1.0]tridecane | HCID 9248 | — |
| Reactant | Lithium iodide | HCID 66321 | — |
| Product | Cyclododecanone | HCID 13246 | 91.2% |
Reaction Steps
Further, Zh. Org. Khim (1990), 26(7), 1497-1500, discloses that when an isomerization reaction of an epoxycyclododecane was carried out in the presence of 2.3 molar % of a catalyst consisting of LiBr (lithium bromide) at a reaction temperature of 150° C. for a reaction time of 10 hours, the target cyclododecanone was obtained at a yield of 96.6%, and when the reaction of the epoxycyclododecane was effected in the presence of 1.5 molar % of LiI (lithium iodide) at 150° C. for 5 hours, the target cyclododecanone was obtained at a yield of 91.2%. In the case of this report, however, it is assumed that to make the conversion of the epoxycyclododecane close to 100%, a very long reaction time is necessary. Also, the reaction of the report was effected in a batch-type reaction system, and thus no continuous method for the reaction is disclosed in the report.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06417404B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-afc397386edf4ef6a4ec69bc8b8698db |
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| Source note | uspto-grants-2002_07 |
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