HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl iodide → 10-(2-Propen-1-yl)-2,3-dihydro[1,4]dioxino[2,3-h]quinolin-10-ium Iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | 2,3-Dihydro[1,4]dioxino[2,3-h]quinoline | HCID 68996469 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 10-(2-Propen-1-yl)-2,3-dihydro[1,4]dioxino[2,3-h]quinolin-10-ium Iodide | HCID 68991195 | 85.2% |
Reaction Steps
2,3-Dihydro[1,4]dioxino[2,3-h]quinoline (3.65 g; 19.52 mmol) and allyl iodide (6.52 ml; 39.04 mmol) were refluxed in toluene (50 ml) at 100° C. After 2.5 h more allyl iodide (0.65 ml; 3.9 mmol) was added to the mixture and the reaction continued under the same conditions for a further 0.5 h. The solvent was removed and the tar like product washed with toluene. This was dried under high vacuum overnight to afford the desired product (5.91 g; 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071592B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-96f54fb39bca4ce888b0d6a92af84341 |
| Source note | uspto-grants-2011_12 |