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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Epoxycyclododeca-5,9-dieneHCID 79135—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product13-Oxabicyclo[10.1.0]tridecaneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515185B1
Source datasetuspto-grants-2003_02
ORD IDord-955891e8821f492a87c22b88d4bfbc19
Source noteuspto-grants-2003_02