Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Allyl acetate | HCID 11584 | — |
| Reactant | Tetrafluoroborate | HCID 26255 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Phenol | HCID 996 | — |
| Product | Allyl phenyl ether | HCID 74458 | — |
Reaction Steps
A mixture of bis(1,5-cyclooctadiene)iridium tetrafluoroborate [Ir(cod)2]+BF4− (0.01 mmol) and toluene (1.0 ml) was treated with phenol (1 mmol) and allyl acetate (5 mmol) with stirring at 100° C. The reaction mixtures after 5 hours and after 15 hours of the reaction were analyzed by gas chromatography. In the reaction mixture after 5 hours, phenyl allyl ether was formed in a yield of 21% with a conversion from phenol of 23%. In the reaction mixture after 15 hours, phenyl allyl ether was formed in a yield of 51% with a conversion from phenol of 51%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304184B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-64c182f7ea934e3da996f9bcfbb77e07 |
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| Source note | uspto-grants-2007_12 |
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