HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 117951634, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 13184333 | HCID 13184333 | — |
| Product | HCID 117951634 | HCID 117951634 | 94% |
Reaction Steps
Referring to Scheme 4 below, N-(3-methylcyclohexyl)pyrrolidine prepared in Example 2 above was quaternized with methyl iodide in a similar fashion to the procedure described in in example 3. The quaternization afforded the desired N-methyl-N-(3-methylcyclohexyl)pyrrolidinium iodide in 94% yield. The resulting iodide salt was exchanged with Bio-Rad AG 1-X8 ion-exchange resin as described in example 3 to give N-methyl-N-(3-methylcyclohexyl)pyrrolidinium hydroxide in 98% yield (titration analysis).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108856B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-3ca60812278b4934a7badcf69bf7d551 |
| Source note | uspto-grants-2015_08 |