HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate → methyl (1S,2R)-2-aminocyclopentane-1-carboxylate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate | HCID 11322482 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl (1S,2R)-2-aminocyclopentane-1-carboxylate hydrochloride | HCID 14698816 | — |
Reaction Steps
To a mixture of methyl (1S,2R)-2-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate (0.84 g) and ethyl acetate (2.5 ml) was added a 4 M hydrogen chloride/ethyl acetate solution (5.0 ml) under ice-cooling, followed by stirring at room temperature for 2.5 hours. The reaction mixture was concentrated under reduced pressure to obtain methyl (1S,2R)-2-aminocyclopentanecarboxylate hydrochloride (0.72 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030489B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-0f6e303c9e86432cbf16bfaff76d4751 |
| Source note | uspto-grants-2011_10 |