HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Trifluoroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 70098694 | HCID 70098694 | — |
| Product | Trifluoroacetate | HCID 84468 | — |
| Product | HCID 70099942 | HCID 70099942 | — |
Reaction Steps
0.25 g of tert-butyl (2R)-2-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonylamino)-3phenylpropionate [obtainable according to Example 12]is stirred in 10 ml of trifluoroacetic acid at room temperature until hydrolysis is complete. The reaction mixture is subsequently concentrated and the residue is washed repeatedly with toluene. Treatment with ethyl acetate gives (2R)-2-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonylamino]-3-phenylpropionic acid, trifluoroacetate, FAB (M+1): 397.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05614535 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-3e68cd002b9a4163bb148e5b9b72231b |
| Source note | uspto-grants-1997_03 |