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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019268Generated: October 28, 2026

cis,cis-1,5-Cyclooctadiene → 5-Decene

https://huagongshe.com/reaction/1019268

Reaction equation

Participants

RoleNameHCIDCharge
Reactantcis,cis-1,5-CyclooctadieneHCID 8135—
Reactant1-HexeneHCID 11597—
CatalystRutheniumHCID 23950—
SolventMethanolHCID 887—
Product5-DeceneHCID 2391620%

Reaction Steps

In contrast to the “classical” ruthenium metathesis catalysts mentioned above, which react only with highly-strained olefins, alkylidenes 6 and 7 of Example 6 also promote the ROMP of less-strained monomers such as 1,5-cyclooctadiene, and are active in the metathesis of acyclic olefins in protic solvents. For example, 6 will dimerize 1-hexene in methanol to give 5-decene in 20% yield (Equation 3). In these systems, separation of catalyst from product is facilitated through addition of water to the reaction mixture. Olefins collected from the resulting two-phase system contain very low levels of detectable ruthenium.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486279B2
Source datasetuspto-grants-2002_11
ORD IDord-d6edd4e4512f4ab9bfc4929ba9a824cd
Source noteuspto-grants-2002_11