HuagongsheHuagongshe Chemistry Print Report · For research reference only
cis,cis-1,5-Cyclooctadiene → 5-Decene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | cis,cis-1,5-Cyclooctadiene | HCID 8135 | — |
| Reactant | 1-Hexene | HCID 11597 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Decene | HCID 23916 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06486279B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-d6edd4e4512f4ab9bfc4929ba9a824cd |
| Source note | uspto-grants-2002_11 |