Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Stearic Acid | HCID 5281 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Glycidyl stearate | HCID 62642 | — |
| Katalysator | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Glyceryl 1,3-distearate | HCID 101269 | — |
Reaktionsschritte
1,3-Disteroylglycerol. A mixture of 171.3 g (0.5 mole) glycidol stearate, 156.5 g (0.55 mole) stearic acid, 1.0 g (0.025 mole) sodium hydroxide, and tetrabutylammonium hydrogensulfate (8.5 g, 0.025 mole) in 400 mL ethanol is heated at reflux (80° C.) for 20 hours. The solid material is removed by passage of the reaction mixture through a short column of silica gel. After evaporation, the crude solid product is subjected to centrifugal partition chromatography using a mixture of acetonitrile-hexane. Recrystallization of the resulting powder from acetone-water gives 1,3-distearoylglycerol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05068119 |
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| Quelldatensatz | uspto-grants-1991_11 |
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| ORD ID | ord-eecbaf9c069c45028570e17526bf5173 |
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| Quellennotiz | uspto-grants-1991_11 |
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