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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt2,3-Bis[(9Z)-9-octadecen-1-yloxy]-1-propanolHCID 5380343—
Edukt4-(Dimethylamino)butyric acid hydrochlorideHCID 12691640—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
Lösungsmitteldichloromethane N,N-dimethylformamideHCID 22350042—
Produkt3-O-(4-dimethylaminobutanoyl)-1,2-O-dioleylglycerolHCID 8675186087,1%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06020317
Quelldatensatzuspto-grants-2000_02
ORD IDord-c3e2d99100fc40ccb67ccb4087237832
Quellennotizuspto-grants-2000_02