HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Ethyl-(1S,2R)-1-amino-2-phenylcyclopropanecarboxylate trifluoroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (1S,2R)-N-Boc-1-amino-2-phenylcyclopropanecarboxylic acid | HCID 7009512 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl-(1S,2R)-1-amino-2-phenylcyclopropanecarboxylate trifluoroacetate | HCID 86678341 | — |
Reaction Steps
The title compound was prepared by standard methods, by esterifying commercially available (1S,2R)-1-[(tert-butoxycarbonyl)amino]-2-phenylcyclopropanecarboxylic acid with ethanol and subsequent Boc detachment with trifluoroacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08992932B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-c93405c8754e4f1882819b8547f69384 |
| Source note | uspto-grants-2015_03 |