HuagongsheHuagongshe Chemistry Print Report · For research reference only
Amantadine → HCID 19427051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Amantadine | HCID 2130 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Product | HCID 19427051 | HCID 19427051 | 2.8% |
Reaction Steps
Adamantyl amine (1.87 g, 10 mmol), triethyl orthoacetate (1.62 g, 10 mmol) and cyclohexyl amine (0.99 g, 10 mmol) were mixed together then placed in preheated oil bath (140° C.) under nitrogen. After 5 min the reaction became exothermic and the reaction mixture became a slurry and upon continuation for 20 min it became a clear colorless solution. Now the reflux condenser was then replaced by distillation condenser and the low volatiles were distilled off at 75°-77° C. (head temperature) and later the undistilled residue was dried on manifold to give a light-yellow solid. The crude product was flash chromatographed on silica gel using chloroform as eluent to afford the title compound (0.076 g, 2.78%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05308869 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-0b577727c2ca4a4ab5322fd7a75b05b3 |
| Source note | uspto-grants-1994_05 |