HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21404613, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21404488 | HCID 21404488 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21404613 | HCID 21404613 | — |
Reaction Steps
A mixture of 9.1 g. of 6-[p-(4-methyl-1-piperazinyl)phenyl]-1,2-dihydro-2-oxonicotinonitrile, 2.0 g. of potassium hydroxide, 5.0 ml. of iodomethane and 250 ml. of absolute ethanol is stirred and heated at reflux for 5 hours, then evaporated at reduced pressure. The residue is washed thoroughly with warm water, then dried, to give 6-[p-(4-methyl-1-piperazinyl)phenyl]-1,2-dihydro-1-methyl-2-oxonicotinonitrile as the remaining solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03951982 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-d636cefa85a4465e90ee41720d58e1a8 |
| Source note | uspto-grants-1976_04 |