HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 19439162, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 10967168 | HCID 10967168 | — |
| Reactant | HCID 19439122 | HCID 19439122 | — |
| Reactant | HCID 54544340 | HCID 54544340 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19439162 | HCID 19439162 | — |
Reaction Steps
A solution of 1 g of ethyl 1-tert-butoxycarbonyl-4-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)piperazine-2-carboxylate (obtainable by reacting 3-(4-cyanophenyl)-5-bromomethyl-2-oxazolidinone with ethyl 1-tert-butoxycarbonylpiperazine-2-carboxylate in accordance with the method described in Example 3) in 12 ml of dichloromethane and 12 ml of trifluoroacetic acid is left to stand at 20° for 1 h. and then concentrated by evaporation. Ethyl 1-(3-(4-cyanophenyl)-2-oxo-5-oxazolidinylmethyl)piperazine-3-carboxylate is obtained, FAB 359.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05532255 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-5453cd3c82b44ffcb76fee8890ecea2f |
| Source note | uspto-grants-1996_07 |