Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Benzyl(E,4S)-4-[(2-hydroxydodecanoyl)amino]oct-2-enoate | HCID 10928405 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10926410 | HCID 10926410 | — |
Reaction Steps
To a solution of benzyl (E,4S)-4-[(2-hydroxydodecanoyl)amino]oct-2-enoate (0.445 g, 1 mmol) in EtOH (2.5 mL), through which N2 had been passed for 5 min, 10% Pd/C catalyst (0.042 g) was added. The reaction mixture was stirred under H2 for 5 h at room temperature. The catalyst was removed by filtration through a pad of Celite and the filtrate was evaporated under reduced pressure. The product was purified by column chromatography (CHCl3/MeOH 9/1). Yield 0.28 g (70%); mp 53-55° C.; [α]D−2.4 (c 0.75 CHCl3); 1H NMR δ 6.82 (1H, m, NH), 4.18 (1H, m, CHNH), 3.91 (1H, m, CHOH), 2.39 (2H, t, J=6.3 Hz, CH2COOH), 1.95-1.12 (26H, m, 13×CH2), 0.88 (3H, t, J=6.0 Hz, CH3); Anal. Calcd. for C20H39NO4: C, 67.19; H, 10.99; N, 3.92. Found: C, 67.05; H, 11.18; N, 3.63.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745489B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-7a8357ff9a39405db8f31c9c82e114da |
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| Source note | uspto-grants-2010_06 |
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