HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21447150, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 57415-52-8 | HCID 12073787 | — |
| Product | HCID 21447150 | HCID 21447150 | — |
Reaction Steps
A mixture of 2.7 g. (0.0063 mole) of finely divided 2,5-bis(2,2,2-trifluoroethoxy)-N-[(1-methyl-2-piperidyl)methyl]-benzamide and 6 ml. of methyl iodide is heated at 56° to 57° C. in a sealed tube for about 90 minutes. The mixtures is extracted with methanol, and the methanol extracts are concentrated to provide a crystalline solid wich is recrystallized from 50 ml. of ethyl acetate and about 2 ml. of isopropanol, with treatment by decolorizing charcoal. The resulting product is dried to provide white solid 2-[2,5-bis(2,2,2trifluoroethoxy)benzamidomethyl]-1,1-dimethylpiperidinium iodide, m.p. 170° -172.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005209 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-8a8b14c3e07e4995bf8f70c369a9dd6f |
| Source note | uspto-grants-1977_01 |