HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-Carboxymethylimidazoline Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | N-Carbobenzyloxymethylimidazoline | HCID 20369282 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Carboxymethylimidazoline Hydrochloride | HCID 20369278 | — |
Reaction Steps
A suspension of 10.9 g. (0.05 mole) of N-carbobenzyloxymethylimidazoline and 50 mg. of 5% palladium-on-charcoal in 100 ml. of ethanol is shaken in an atmosphere of hydrogen at atmospheric pressure. When the theoretical amount of hydrogen has been absorbed, the spent catalyst is filtered and the filtrate treated with one equivalent of hydrogen chloride dissolved in ethyl acetate. The resulting solution is then concentrated to dryness in vacuo and the residual product triturated with ether and filtered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03951952 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-12ee13795c0b4956a3fa5f2fd847ceec |
| Source note | uspto-grants-1976_04 |