HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclododecanone → 13-Oxabicyclo[10.1.0]tridecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclododecanone | HCID 13246 | — |
| Catalyst | Lithium Chloride | HCID 433294 | — |
| Product | 13-Oxabicyclo[10.1.0]tridecane | HCID 9248 | 94% |
Reaction Steps
For example, German Patent (DE) No. 3,601,380 discloses a method in which cyclodeca-3,7-diene-1-one is produced in a yield of 98.7% by an isomerization reaction of 1,2-epoxycyclododeca-5,9-diene in the presence of sodium iodide catalyst in a reaction medium consisting of polyethyleneglycol. Also, German Patent (DE) No. 3,744,094 discloses a method in which cyclododecanone is produced in a yield of 94% by an isomerization reaction of an epoxycyclododecane in the presence of a lithium chloride catalyst in a reaction medium consisting of N-methylpyrrolidone and/or N,N′-dimethylethyleneurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06388140B2 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-a2bdeb50b55b4681b2e8a0e5d66e4973 |
| Source note | uspto-grants-2002_05 |