HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl iodide → 6-Fluoro-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 | 6-Fluoro-2,3-dihydro[1,4]dioxino[2,3-h]quinoline | HCID 68993398 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Fluoro-10-(2-propen-1-yl)-2,3-dihydro[1,4]dioxino[2,3-h]quinolin-10-ium Iodide | HCID 68991223 | 80% |
Reaction Steps
6-fluoro-2,3-dihydro[1,4]dioxino[2,3-h]quinoline (2.78 g, 13.6 mmol) and allyl iodide (2.5 ml, 27.2 mmol) in toluene (50 ml) under argon was heated at 90° C. than at 120° C. for 5 h. The reaction was cooled to rt, the solvent decanted and the solid dried in the vacuum oven at 40° C. overnight to afford the desired product (4 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071592B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-ebde29b9ef2b485a86970b50960c3ff4 |
| Source note | uspto-grants-2011_12 |