Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | 7-Methoxyquinoline | HCID 78666 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68811156 | HCID 68811156 | 82.2% |
Reaction Steps
7-(Methyloxy)quinoline (8.76 g; 55.09 mmol) and allyl iodide (19.72 ml; 110.18 mmol) were refluxed in toluene (120 ml) at 95° C. for 1 h, more allyl iodide (9.86 ml; 55.09 mmol) was added and the temperature of the reaction increased to 110° C. After a further 1 h the temperature of the reaction was increased to 120° C. and reaction continued for a further 0.5 h. The solvent was removed under vacuum and the resulting brown solid was washed with toluene and diethyl ether. The resultant solid were left to dry in a vacuum oven overnight to give the desired product (14.81 g; 82%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071592B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-15d72a5f88124eb5a0b02bcf6a96b9ec |
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| Source note | uspto-grants-2011_12 |
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