HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 70591612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Carbobenzoxy-L-valine | HCID 726987 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Reactant | Methanesulfonic acid, 1H-benzotriazol-1-yl ester | HCID 11745953 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70591612 | HCID 70591612 | 58.8% |
Reaction Steps
N-Benzyloxycarbonyl-L-valine (1.26 g), glycine ethyl ester hydrochloride (0.70 g) and triethylamine (1.40 ml) are dissolved in anhydrous chloroform (10 ml), and thereto is added 1-methanesulfonyloxy-1,2,3-benzotriazole (1.05 g) with stirring under ice-cooling. After stirrig at room temperature for 20 hours, to the reaction mixture are added water and ethyl acetate. The ethyl acetate layer is separated, washed and dried. After drying, the solvent is distilled off to give N-(N-benzyloxycarbonyl-L-valyl)glycine ethyl ester hydrochloride (1.1 g), melting point: 162°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242507 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-8f6f15c0d46a441da51fbe7d11fe13c1 |
| Source note | uspto-grants-1980_12 |