Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21832279 | HCID 21832279 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 11790368 | HCID 11790368 | — |
Reaction Steps
To a solution of α-amino-β-hydroxy-β-phenylpropane nitrile bisulphate salt (6 g, 23 mmoles) in 50 ml MeOH/H2O (m:m/1:1) triethylamine (TEAM) (9.6 g, 69.2 mmoles) was added. Subsequently, for 6 hours CO2 was bubbled through the solution at 40° C. During the reaction the pH of the solution fell from 9.7 to 7.8. A white solid substance crystallized out of the solution. This substance was filtered off and dried in a vacuum. The yield was 4.7 g (22.8 moles, 99 wt. % ), obtained in the form of white crystals having a melting point: 249-250° C.; 1H NMR (200 MHz, DMSO) d (ppm): 3.30 (0.5H, s, H2O), 4.42 (1H, δ, J=8.37 Hz, NCHCO), 5.79 (1H, d, J=8.37 Hz, OCHPh), 6.85 (1H, s, NH), 7.20 (1H, s, NH), 7.30 (5H, m, Ph), 8.00 (1H, s, NH); 13C NMR (200 MHz, DMSO) δ (ppm): 59.41 (NCHCO), 78.75 (OCHHPh), 126.82 (Ph), 127.94 (Ph), 128.41 (Ph), 135.44 (Ph), 15.02 (NC=OO), 169.77 (C=ONH2); IR (KBr,cm-1): 3396 (NH2), 3273 (NH2), 3200, 1740 (C=O), 1719, 1684 (C=O), 1611 Mass (El): 206 M, 189, 163, 105, 77, 44. The experiment was repeated under different conditions. The results are shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977406 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-80a8df74653c4d5297bae34d4b0316db |
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| Source note | uspto-grants-1999_11 |
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