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 (240.03 g, 3113.9 mmol) was added to a solution of (R)-ethyl 2-methyl-5-oxocyclopentanecarboxylate (106.0 g, 622.78 mmol) in MeOH (1.2 L). The reaction mixture was stirred at room temperature under nitrogen for 20 hours, after which it was complete as judged by TLC and HPLC. The reaction mixture was concentrated to remove MeOH. The resulting residue was dissolved in DCM, washed twice with H2O, once with brine, dried (Na2SO4), filtered, and concentrated to give (R)-ethyl 2-amino-5-methylcyclopent-1-enecarboxylate (102 g, 97% yield) as an orange oil. LC/MS (APCI+) m/z 170 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150549B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-44fcf746e47446ec8f3ee31763e90255 |
| Source note | uspto-grants-2015_10 |