HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Trimethyl(4-hydroxy-3-methoxy-5-methylbenzyl)ammonium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 10382346 | HCID 10382346 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Trimethyl(4-hydroxy-3-methoxy-5-methylbenzyl)ammonium iodide | HCID 20634507 | 98% |
Reaction Steps
To a dioxane solution (600 ml) of dimethyl(4-hydroxy-3-methoxy-5-methylbenzyl)amine (98 g, 0.50 mol) was added methyl iodide (69 ml, 1.11 mol) and the resulting mixture was refluxed for 2 h. The solid formed was filtered and washed with dioxane to yield 165 g (98%) of the trimethyl(4-hydroxy-3-methoxy-5-methylbenzyl)ammonium iodide salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706698B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-6362949ddcbb42adb9ac3daf20f78de4 |
| Source note | uspto-grants-2004_03 |