HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058207Generated: October 31, 2026
1,2-Epoxycyclododeca-5,9-diene → 13-Oxabicyclo[10.1.0]tridecane
https://huagongshe.com/reaction/1058207
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Epoxycyclododeca-5,9-diene | HCID 79135 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 13-Oxabicyclo[10.1.0]tridecane | HCID 9248 | — |
Reaction Steps
As a process for producing cyclododecanone and cyclododecanol by a catalytic reaction of epoxycyclododecane compounds with hydrogen, J. Mol. Catal., Vol 169, pp 95-103 (1991) discloses a catalytic hydrogenating reaction of 2-epoxy-5,9-cyclododecadiene with hydrogen. In this reaction of the reference, 1,2-epoxy-5,9-cyclododecadiene is brought into contact with hydrogen in the presence of a palladium-carrying catalyst at a reaction temperature of 90° C. under a hydrogen gas pressure of 1,275 kPa (13 kg/cm2) on gauge, and epoxycyclododecane is produced as a principal reaction product. Cyclododecanol is produced as a by-product in a yield of 4% and no cyclododecanone is produced. Also, the Draft of 24-th Symposium “Development of Reaction and Synthesis, Nov. 5-6, 1998, pp 68, discloses a process of catalytic reaction of 1,2-epoxy-5,9-cyclododecadiene with hydrogen in the presence of a palladium catalyst at room temperature under the ambient atmospheric pressure. In this process, epoxycyclododecane is produced as a principal product, cyclododecanol is produced, as a by-product, in a yield of 5%, and no cyclododecanone is produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515185B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-955891e8821f492a87c22b88d4bfbc19 |
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| Source note | uspto-grants-2003_02 |
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