HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-(diphenylmethyl)-1-N-(n-dodecyliminomethyl)piperidine fumarate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Dodecylamine | HCID 13583 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Fumarate | HCID 5460307 | — |
| Reactant | 4-(Diphenylmethyl)-1-piperidinecarbothioaldehyde | HCID 13097878 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(diphenylmethyl)-1-N-(n-dodecyliminomethyl)piperidine fumarate | HCID 20291226 | — |
Reaction Steps
A solution of 5.54 g (0.019 mole) of 4-(diphenylmethyl)-1-piperidinecarbothioaldehyde in 20 ml of chloroform was treated with 2.65 g (1.16 ml, 0.019 mole) of methyl iodide and refluxed for one hour. The resulting solution was treated with 3.49 g (0.019 mole) of n-dodecylamine, refluxed one and one half hours, cooled, treated with aqueous sodium hydroxide and the organic layer separated. After drying, evaporation yielded an oil which was converted to the fumarate to yield 4-(diphenylmethyl)-1-N-(n-dodecyliminomethyl)piperidine fumarate; m.p. 143°-145.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251655 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-0d6cffce02a649ea93587ddd40a8a621 |
| Source note | uspto-grants-1981_02 |