HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → ethyl (1S,2R)-2-aminocyclopentanecarboxylate trifluoroacetic acid salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (1R,2S)-2-(Boc-amino)cyclopentanecarboxylate | HCID 6978750 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl (1S,2R)-2-aminocyclopentanecarboxylate trifluoroacetic acid salt | HCID 131734488 | — |
Reaction Steps
(1R,2S)-2-(Boc-amino)cyclopentanecarboxylate (CAS: 1140972-29-7, TCI) (1 mmol) was dissolved in CH2Cl2 (3 mL) followed by the slow addition of TFA (1 mL) at 0° C. The reaction mixture was stirred at rt for 1 hour and then the solvent was removed under vacuum to give the crude product 50-B, which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09233978B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-c0904c3f1174464493ccfb2419600743 |
| Source note | uspto-grants-2016_01 |