HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[(Benzyloxy)carbonyl]glycylglycinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(Benzyloxy)carbonyl]glycylglycinamide | HCID 297865 | 50% |
Reaction Steps
N-benzyloxycarbonylglycine (3 g, 14.4 mmole) were dissolved in 200 mL of dichloromethane and 4.5 g (21.6 mmole) of DCC were added. The mixture was stirred at room temperature for 2 hours, the insoluble materials were removed and 3.2 g (28.8 mmole) of glycinamide hydrochloride and 2.93 g (28.8 mmole) of TEA (triethylamine) were added to the filtrate. The reaction was stirred for 24 hours at room temperature, the insoluble materials were filtered and the filtrate was evaporated to dryness in vacuum. The residue was recrystallized from distilled water to get a pure product 1.9 g (7.2 mmole), yield of 50%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06028102 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-5520e2a0fd7c4403a09eeac5a8c54fd2 |
| Source note | uspto-grants-2000_02 |