HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → methyl N-benzyloxycarbonylglycinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | HCID 54246101 | HCID 54246101 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | methyl N-benzyloxycarbonylglycinate | HCID 71033 | — |
Reaction Steps
To a solution of N-benzyloxycarbonylglycine (1.05 g) and triethylamine (0.7 ml) in chloroform (10 ml) and acetonitrile (5 ml), 2-methoxycarbonyloxyimino-2-cyanoacetic acid amide (0.85 g) is added, and the resulting mixture is stirred at room temperature for 1 hour and allowed to stand over night. The reaction mixture is treated as in Example A to give N-benzyloxycarbonylglycine methyl ester (1.1 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976635 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-a6ff67c2293049cdbe48b468b27a72ff |
| Source note | uspto-grants-1976_08 |