HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Aminomethyl-1-ethyl-1,2,3,6-tetrahydropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Acetylaminomethyl-1-ethyl-1,2,3,6-tetrahydropyridine | HCID 15023457 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Aminomethyl-1-ethyl-1,2,3,6-tetrahydropyridine | HCID 15023458 | 92.6% |
Reaction Steps
A solution of 4-acetylaminomethyl-1-ethyl-1,2,3,6-tetrahydropyridine (20.0 g) and 6N aqueous solution of sodium hydroxide (73 ml) in methanol (150 ml) was refluxed for 40 hours. The solution was acidified with concentrated hydrochloric acid under ice cooling and evaporated in vacuo. To the residue was added ethanol (400 ml) and the mixture was refluxed for an hour. The resulting precipitates were filtered off and the filtrate was evaporated in vacuo. The residue was treated with Amberlite IRA-910 (trademark: Rohm & Haas Co.) and purified by vacuum distillation to give 4-aminomethyl-1-ethyl-1,2,3,6-tetrahydropyridine (14.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05066680 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-fe3df2e00a644707aa404ea53cedf97d |
| Source note | uspto-grants-1991_11 |