Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Trioctadecylamine | HCID 458429 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 10485970 | HCID 10485970 | — |
Reaktionsschritte
N-(3β-cholestanyl)-N-methyl-N,N-dioctadecylammonium chloride of the formula (VIII): ##STR16## The gelators of Examples VI-IX are synthesized by the following procedures. N-methyl-N,N,N-trioctadecylammonium iodide is prepared according to the following process. 0.10 g (0.13 mmol) trioctadecylamine is dissolved in 1.5 ml THF (certified grade, Fisher), and 0.1 ml (1.6 mmol) CH3I (99%, Aldrich) is placed in the above solution. The solution is stirred in a nitrogen atmosphere at 38°-40° C. for 3 h. 95 mg (80%) white solid, mp 108°-111° C., is obtained after the solvent is evaporated under house vacuum pressure, and the residue is recrystallized in ethanol (anhydrous). IR (KBr) 2917, 2859 (C-H stretching, vvs), 1473 (C-H bending, w) cm-1. 1HNMR (CDCl3) δ 3.52-3.38 (CH2, m, 6H), 3.31 (CH3, s, 3H), 1.76-0.82 (heptadecyl groups, m, 105H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05892116 |
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| Quelldatensatz | uspto-grants-1999_04 |
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| ORD ID | ord-9a00909e838746b6991426c83bac4f62 |
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| Quellennotiz | uspto-grants-1999_04 |
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