HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-cyano-3-phenylpropanoate → Ethyl 3-amino-2-benzylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-cyano-3-phenylpropanoate | HCID 228103 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-amino-2-benzylpropanoate | HCID 19611763 | — |
Reaction Steps
The resulting ethyl benzylcyanoacetate was dissolved in 200 ml of EtOH and hydrogenated over Raney nickel. After removal of the catalyst by filtration with suction and concentration, 8.2 . . . of oil were obtained, and chromatography over silica gel (EA to EA/MeOH 5/1) gave 5.5 g of ethyl 3-amino-2-benzylpropionate. This compound was reacted with Boc2O to give ethyl 2-benzyl-3-(tert.-butoxycarbonylamino)-propionate, which was hydrolyzed, and the product was coupled with H-Val-OMe by the PPA method. The resulting diastereomers were resolved by chromatography (toluene/diisopropyl ether 1/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05712417 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-90bd783a37ef46e9a04450fc5a2839c3 |
| Source note | uspto-grants-1998_01 |