Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Reactant | HCID 10586976 | HCID 10586976 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | HCID 9864811 | HCID 9864811 | 124.3% |
Reaction Steps
To a stirred solution of 3-amino-3-(3',4'-diethoxyphenyl)propionic acid (1.03 g, 4.07 mmol) and sodium carbonate (0.453 g, 4.27 mmol) in a 1/1 mixture of 150 mL of acetonitrile/water (heated to 45 C to dissolve) was added N-carbethoxyphthalimide (0.89 g, 4.07 mmol). The reaction mixture was stirred 1 h, then partially concentrated in vacuo to remove the acetonitrile to afford a pale yellow solution. The stirred solution was acidified to pH 0-1 with 4N hydrochloric acid to form a gum. The mixture was stirred overnight. The gum had not solidified, 1 mL of ether was added to mixture. The gum solidified on stirring, the slurry was filtered and the solid dried to afford 1.94 g (94%) of 3-(3',4'-diethoxyphenyl)-3-phthalimidopropionic acid as a yellow solid: 1H NMR (DMSO-d6, 250 MHz) 12.41 (br s, 1 H, COOH), 8.10-7.75 (m, 4 H, Ar), 7.15-6.85 (m, 3 H, Ar), 5.62 (overlapping dd, 1 H), 4.20-3.90 (m, 4 H, 2 OCH2), 3.51 (dd, 1 H, J=16.5, 9 Hz), 3.25 (dd, 1 H, J=16.5, 7 Hz), 1.5-0.9 (m, 6 H, 2 CH3) 13C NMR (DMSO-d6) 1717, 167.6, 147.9, 147.8, 134.6, 131.3, 131.0, 123.1, 119.4, 113.2, 112.7, 63.8, 63.7, 50.0, 36.0, 14.6, 14.6; Anal. Calcd for C21H21NO6 : Theory C, 65.79; H, 5.52; N, 3.65. Found: C, 65.54; H, 5.55; N, 3.62.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05605914 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-c8af4919582c47539ef4fa2d9e8b68c2 |
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| Source note | uspto-grants-1997_02 |
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