HuagongsheHuagongshe Chemistry Print Report · For research reference only
Amantadine → N-(Adamantan-1-yl)prop-2-enimidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Amantadine | HCID 2130 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(Adamantan-1-yl)prop-2-enimidic acid | HCID 284637 | — |
Reaction Steps
A solution of acryloyl chloride (4.05 ml, 0.05 mole) in ethyl ether (25 ml) was added to a cold (+5° C.) solution of 1-adamantaneamine (7.65 g, 0.05 mole) and triethylamine (15.3 ml, 0.11 mole) in ethyl ether (300 ml) and the solution stirred for 72 hours at room temperature. The solvent was removed on a rotary evaporator. The residue was dissolved in ethyl acetate (100 ml), washed with 10 percent hydrochloric acid (100 ml) and water (50 ml), dried over sodium sulfate, filtered and the solvent removed in vacuo leaving an oily solid which was crystallized from methanol-ethyl acetate-hexane. The structure was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05157053 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-70ddae7078dc46be975f7612e78cc370 |
| Source note | uspto-grants-1992_10 |