HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 18008655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Piperidine, 1-((-phenylcyclopentyl)methyl)- | HCID 566548 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18008655 | HCID 18008655 | 96.6% |
Reaction Steps
To a mechanically stirred solution of [(1-phenylcyclopentyl)methyl]piperidine (115 gm; 0.47 mole) in 1000 ml methanol (ACS reagent), methyl iodide (100 gm; 0.7 mole) were added. The resulting mixture was stirred for 48 hrs. Then an additional 35 gm (0.5 mole equivalent) of methyl iodide was added and the reaction was heated for 1 hr. The resulting solution was concentrated under reduced pressure on a rotary evaporator to give 175 gm of a tan solid material. The obtained solid was re-crystallized by dissolving in hot isopropyl alcohol and allowed to re-crystallize overnight. Re-crystallization afforded 171 gm of the product (NMR analysis) as shinny white needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06461578B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-8fa7999e1deb4a8fa41ede6168b6b113 |
| Source note | uspto-grants-2002_10 |