HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl iodide | HCID 12098 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | HCID 178506446 | HCID 178506446 | — |
| Product | Quinoline | HCID 7047 | — |
Reaction Steps
To the solution is added one equivalent to a small excess amount of a base, e.g. potassium carbonate, triethylamine, sodium hydrogen, one equivalent to excess amount of halogens alkyl derivative, e.g. methyl iodide, propyl iodide, benzyl iodide, and the mixture is stirred at a temperature of 0° C. to 80° C. to give a quinoline derivative (ivz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06015789 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-fca95870832c4d87b38e4a935aee1564 |
| Source note | uspto-grants-2000_01 |