HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 376423Erstellt: 24. Oktober 2026
Dicyclohexylcarbodiimide → 3-O-(4-dimethylaminobutanoyl)-1,2-O-dioleylglycerol
https://huagongshe.com/de/reaction/376423
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 2,3-Bis[(9Z)-9-octadecen-1-yloxy]-1-propanol | HCID 5380343 | — |
| Edukt | 4-(Dimethylamino)butyric acid hydrochloride | HCID 12691640 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Produkt | 3-O-(4-dimethylaminobutanoyl)-1,2-O-dioleylglycerol | HCID 86751860 | 87,1% |
Reaktionsschritte
In 6 ml of methylene chloride-N,N-dimethylformamide (1:2) was dissolved 120 mg (0.20 mmol) of 1,2-O-dioleylglycerol, followed by addition of 168 mg (1 mmol) of 4-dimethylaminobutyric acid hydrochloride. Then, 206 mg (1 mmol) of N,N'-dicyclohexylcarbodiimide (DCC) and 25 mg (0.2 mmol) of 4-dimethylaminopyridine were further added and the reaction was conducted at ambient temperature overnight. The precipitated byproduct urea was filtered off using a glass filter and the filtrate was concentrated to dryness under reduced pressure and treated with methylene chloride-saturated aqueous sodium hydrogen carbonate solution. After phase separation, the methylene chloride layer was dried over sodium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to column chromatography (silica gel/methylene chloride-methanol) to provide 123 mg (87%) of the title compound of the invention.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06020317 |
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| Quelldatensatz | uspto-grants-2000_02 |
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| ORD ID | ord-c3e2d99100fc40ccb67ccb4087237832 |
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| Quellennotiz | uspto-grants-2000_02 |
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