HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → Ethyl (5R)-2-amino-5-methyl-1-cyclopentene-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | (R)-ethyl 2-methyl-5-oxocyclopentanecarboxylate | HCID 86618740 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl (5R)-2-amino-5-methyl-1-cyclopentene-1-carboxylate | HCID 59671147 | 97% |
Reaction Steps
Ammonium acetate (240 g, 3114 mmol) was added to a solution of (R)-ethyl 2-methyl-5-oxocyclopentanecarboxylate (106.0 g, 622.8 mmol) in MeOH (1.2 L). The reaction mixture was stirred at room temperature under nitrogen for 20 hours, and the reaction was complete as determined by TLC and HPLC. The reaction mixture was concentrated to remove MeOH. The resulting residue was dissolved in DCM, washed with H2O (2×), brine (1 X), dried (Na2SO4), filtered, and concentrated to give (R)-ethyl 2-amino-5-methylcyclopent-1-enecarboxylate (102 g, 97% yield) as an oil. LC/MS (APCI+) m/z 170 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853216B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-51cb5c55a9e841cf99960099c3c2459c |
| Source note | uspto-grants-2014_10 |