Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Octanedioyl dichloride | HCID 534653 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Octanedioic Acid Benzylamide | HCID 23092300 | — |
Reaktionsschritte
To a stirred solution of suberoyl chloride (1.00 mL, 5.55 mmol) in THF (40 mL) at 0° C. was added a solution of benzylamine (0.61 mL, 5.55 mmol) and DIEA (1.45 mL, 8.33 mmol) in THF (10 mL) dropwise. The mixture was allowed to warm to ambient temperature and stirred for 1 h. Then, HCl (10 mL, 1 N) was added and the mixture stirred for 0.5 h. The contents were diluted with EtOAc (30 mL) and the layers separated. The aqueous portion was extracted with EtOAc (3×10 mL), the organics combined, washed with brine (5 mL), and dried over MgSO4. Filtration and concentration under reduced pressure left 49 as an off-white solid. 1H-NMR (300 MHz, DMSO-d6) δ 11.98 (br s, 1H), 9.80 (t, 1H), 7.32 (m, 2H), 7.23 (m, 3H), 4.25 (d, 2H), 2.19 (t, 2H), 2.12 (t, 2H), 1.50 (m, 4H), 1.25 (m, 4H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06511990B1 |
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| Quelldatensatz | uspto-grants-2003_01 |
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| ORD ID | ord-08a6c6be81e84633aa1ec01bd1308185 |
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| Quellennotiz | uspto-grants-2003_01 |
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