HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-[(Ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 4-[(Ethylthio)methyl]pyridine | HCID 14442205 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[(Ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridine | HCID 14442215 | 47.6% |
Reaction Steps
8.2 g (0.054 mol) of 4-[(ethylthio)methyl]pyridine are dissolved in 60 ml of acetonitrile and then 9.1 g of methyliodide are added. After 12 hours the reaction mixture is evaporated down in vacuo. The residue is reacted analogously to Example 1 b) with sodium borohydride in methanol and worked up. The crude product obtained is distilled (5.2 g; 56.3% of theory; b.p. 118°-120° C./20 mbar) and then chromatographed on neutral aluminium oxide using chloroform as eluant. 4.4 g of 4-[(ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridine are obtained, which is converted with one equivalent of maleic acid into the maleate (m.p. 102°-105° C., from ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05422353 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-833ce92ccfa44f91b77719638dad4bee |
| Source note | uspto-grants-1995_06 |