HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl iodide → HCID 68993985, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | Quinoline-7-carbonitrile | HCID 22344048 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68993985 | HCID 68993985 | 82.3% |
Reaction Steps
7-Quinolinecarbonitrile (1.01 g, 6.6 mmol) and allyl iodide (1.2 mL, 13.2 mmol) in toluene (10 ml) was heated at 90° C. then at 120° C. for 2 h. More allyl iodide was then added (1.2 ml, 13.2 mmol). After other 2 h more allyl iodide was added (1.2 ml, 13.2 mmol). After 2 h more the reaction was cooled to rt. The solid was filtered off, washed with toluene and dried in vacuo at 45° C. overnight to afford the desired compound (1.75 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071592B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-31651089a8744f9b90a1ab9511b6e2c9 |
| Source note | uspto-grants-2011_12 |