HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Carbethoxyphthalimide → (S)-2-phthalimido-3-phenylpropionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Reactant | Phenylalanine amide hydrochloride | HCID 11953719 | — |
| Product | (S)-2-phthalimido-3-phenylpropionamide | HCID 765708 | — |
Reaction Steps
By following the procedure of Example 19 but employing N-carbethoxyphthal imide and (S)-phenylalaninamide hydrochloride, there is obtained (S)-2-phthalimido-3-phenylpropionamide which can be recrystallized from ethanol to afford white crystals: mp 211°-215° C.; 1H NMR (DMSO-d6) δ 7.92 (s, 5 H, Ph), 7.72, 7.33 (2 s, 2 H), 7.2-7.0 (m, 4 H, Ar), 4.92 (dd, 1 H, J=12, 4.5 Hz), 3.52 (dd, 1 H, J=4.3, 13.9), 3.35 (dd, 1 H, J=12, 13.9); 13C NMR (DMSO-d6) δ 169.6, 167.4, 137.7, 134.3, 131.2, 128.5, 128.1, 126.3, 122.9, 54.2, 33.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05605914 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-9a500af93fad4ee887e7d6e855a47f92 |
| Source note | uspto-grants-1997_02 |