HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → ethyl 1-[(2R)-2-amino-2-phenylethyl]piperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | ethyl 1-{(2R)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl}piperidine-4-carboxylate | HCID 86713423 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 1-[(2R)-2-amino-2-phenylethyl]piperidine-4-carboxylate | HCID 86713422 | 102.2% |
Reaction Steps
To a solution of 160 mg of ethyl 1-{(2R)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl}piperidine-4-carboxylate in 1.5 mL of dichloromethane was added 0.7 mL of trifluoroacetic acid, followed by stirring for 1 hour. The solvent was evaporated under reduced pressure, and a saturated aqueous sodium carbonate solution and a chloroform-methanol mixed solution were added thereto in this order to carry out a layer separation operation. After drying over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure to obtain 120 mg of ethyl 1-[(2R)-2-amino-2-phenylethyl]piperidine-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447090B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-b23b9a5ade5d484686cc78efe268cc66 |
| Source note | uspto-grants-2016_09 |