Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Beta-Alanine | HCID 239 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Boc-Leu-OSu | HCID 11023929 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 14562633 | HCID 14562633 | — |
Reaktionsschritte
Boc-L-Leu-OSu (5 g, 15.24 mmol) was dissolved in a solution (200 ml) containing equal volumes of tetrahydrofuran and 5% Na2CO3. β-Alanine (2.71 g, 30.48 mmol) was added and the reaction mixture was stirred at room temperature for 4 hours. The organic solvent was removed in vacuo and the resulting aqueous solution was washed with diethyl ether (2×50 ml). On acidification with 5% NaHSO4, the product precipitated and was extracted into ethyl acetate (150 ml). The organic layer was washed with brine and dried over magnesium sulphate. On reduction to dryness, Boc-Leu-β-Ala was initially obtained as a clear oil but on standing at -20° C., formed an amorphous solid. The product was judged homogeneous by tlc in chloroform/methanol (4:1) (Rf 0.514) or chloroform/methanol (1:1) (Rf 0.554). Yield 2.89 g (63%), m.p. 91°-92° C. (Found: C, 55.61; H, 8.61; N, 9.29. C14H26O5N2 requires C, 55.63; H, 8.61; N, 9.27%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04997950 |
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| Quelldatensatz | uspto-grants-1991_03 |
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| ORD ID | ord-82b45e7055904f02b365e821adf44cfe |
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| Quellennotiz | uspto-grants-1991_03 |
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