HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1,3,4-Trimethylpyridin-1-ium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3,4-Dimethylpyridine | HCID 11417 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,3,4-Trimethylpyridin-1-ium iodide | HCID 12543166 | — |
Reaction Steps
As shown in Scheme 2 (in FIG. 2), a solution of 100 g of 3,4-dimethylpyridine in 800 ml of acetone was added dropwise to 57.27 mL of methyl iodide. The reaction mixture was stirred at room temperature for 18 hrs. The solid was collected by filtration and washed with cold ether. After drying under vacuum, there was obtained 202 g of 1,3,4-trimethylpyridinium iodide. The subsequent Grignard reaction was conducted under standard conditions to afford an unstable intermediate that was utilized immediately.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05354758 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-ce38c26ff9634aa1870c0c0115da3771 |
| Source note | uspto-grants-1994_10 |