Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromooctadecane | HCID 8218 | — |
| Edukt | Propanedioic acid, dibutyl ester | HCID 136925 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | Dibutyl distearylmalonate | HCID 53741587 | — |
Reaktionsschritte
62 m mol of dibutyl malonate, 63 m mol of stearyl bromide, and 69 m mol of sodium were made to react in butanol in the presence of 2 m mol of a crown ether, thereby forming 30 m mol of dibutyl distearylmalonate. Dibutyl distearylmalonate, 15 m mol, was first hydrolyzed, and was then heated in vacuum to be decarboxylated, whereby obtaining 10 m mol of 2-octadecyl eicosanoic acid. This acid, 8 m mol, was converted into its acid chloride. The acid chloride was allowed to react with 10 m mol of p-amino-methlylsulfonylanilide in pyridine, thereby obtaining 7 m mol of p-methylsulfonamide-3-heptadecyleicosanoylanilide. The eicosanoylanilide, 5 m mol, was allowed to react with lead tetraacetate in toluene, thus forming 3.2 m mol of N-(2-octadecyleicosanoyl)-N'methylsulfonyl-p-quinonediimine which is represented by the following formula: ##STR29##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05153680 |
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| Quelldatensatz | uspto-grants-1992_10 |
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| ORD ID | ord-fd0abdadef38452ba9ba8e7192e74532 |
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| Quellennotiz | uspto-grants-1992_10 |
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