HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 86605588, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 18001144 | HCID 18001144 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86605588 | HCID 86605588 | 61.5% |
Reaction Steps
To a solution of 1-benzyl-3-o-tolyl-piperidine-4-one (5165 mg) in acetone (25 ml) was slowly added methyl iodide (3048 mg) at room temperature. The solution was stirred at room temperature over night. A white solid precipitated and was filtered off. The solid was washed four times with 50 ml of acetone and dried under reduced vacuum. The filtrate was evaporated and the residue was stirred with ethyl acetate. The white solid was filtered, washed with ethyl acetate and dried under vacuum. The two solids were combined to yield 1-benzyl-3-butyl-1-methyl-4-oxo-piperidinium iodide as a yellowish solid (4400 mg). MS (ESI): 294.3 (M−I−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07683079B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-7f40de31d55446a48d2a191f11c2e689 |
| Source note | uspto-grants-2010_03 |