HuagongsheHuagongshe Chemistry Print Report · For research reference only
Beta-Alanine → HCID 14557735, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Beta-Alanine | HCID 239 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 53863562 | HCID 53863562 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14557735 | HCID 14557735 | — |
Reaction Steps
The solution of 1.5 g of 3-aminopropionic acid and 1.8 g of sodium carbonate in 30 ml of water at 0° is added to 2.2 g of 4-ethoxycarbonyl-(R*,R*)-2,4-dibenzylbutyryl chloride and the mixture is stirred at room temperature for 4 hours. The mixture is extracted with ether, and the aqueous layer is acidified with 2N hydrochloric acid. The acidic solution is extracted with ethyl acetate, washed with saturated brine, dried (magnesium sulfate), filtered and concentrated. The residue is recrystallized from ether to yield N-[4-ethoxycarbonyl-(R*,R*)-2,4-dibenzylbutyryl]-3-aminopropionic acid, melting at 84°-86°; NMR (CDCl3) δ10.5 (1H, CO2H), 6.1 (t, 1H, J=6 Hz, NH), 4.1 (q, 2H, J=8 Hz, OCH2), 1.08 (t, 3H, J=8 Hz, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05096925 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-8d5d789a215443ca83e48668db3181e1 |
| Source note | uspto-grants-1992_03 |