HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminoazepan-2-one hydrochloride → Lysine ethyl ester dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminoazepan-2-one hydrochloride | HCID 12228562 | — |
| Reactant | Ethyl L-lysinate monohydrochloride | HCID 18600938 | — |
| Reactant | Ethanol sodium ethoxide | HCID 23706232 | — |
| Product | Lysine ethyl ester dihydrochloride | HCID 107468 | 40% |
Reaction Steps
The contents, taken out from the glass ampule, were neutralized to about pH 8.0 by adding sodium ethylate-ethanol solution, and the mixture of α-amino-ε-caprolactam hydrochloride, lysine ethyl ester monohydrochloride, and a small amount of lysine ethyl ester dihydrochloride, was obtained. α-amino-ε-caprolactam hydrochloride, lysine ethyl ester dihydrochloride, and sodium chloride were eluted by passing the mixture through the weak cation exchange column, Amberlite IRC-50, freed from water before use, and washing the column with ethanol. Then, 1.18 grs. of lysine ethyl ester monohydrochloride was eluted in the form of the dihydrochloride salt by charging ethanolic hydrochloride into the weak cation exchange column. (yield 40%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04154956 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-0562b5396eec45c583160c9d9868a9bd |
| Source note | uspto-grants-1979_05 |