HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(1-Carboxycyclopentyl)-2-aminopropanoic acid t-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(1-Carboxycyclopentyl)-2-(dibenzylaminomethyl)propanoic acid t-butyl ester hydrochloride | HCID 70047566 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(1-Carboxycyclopentyl)-2-aminopropanoic acid t-butyl ester | HCID 54352434 | — |
Reaction Steps
3-(1-Carboxycyclopentyl)-2-(dibenzylaminomethyl)propanoic acid t-butyl ester hydrochloride (20.0 g; 41 mmol) in ethanol (160 ml) and triethylamine (2.0 ml) was hydrogenated over palladium (from 20% Pd(OH)2 /C; 20 g) at 60 p.s.i. (4.1 bar). After eighteen hours the mixture was filtered through arbicel, the solvent evaporated and the residue dried azeotropically with toluene. The required primary amino acid triethylamine salt, containing one mole equivalent of triethylamine hydrochloride was thus obtained as a white solid (16.21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960792 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-0fa2c1cde6e246bfb9d368795db5fcb7 |
| Source note | uspto-grants-1990_10 |