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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1196069Erstellt: 25. Oktober 2026

Triethylamine → N-oleoyl-D-serine

https://huagongshe.com/reaction/1196069

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktD-SerineHCID 71077—
EduktOleic AcidHCID 445639—
Edukt4-Hydroxyphenyldimethylsulfomethyl sulfateHCID 86745786—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-oleoyl-D-serineHCID 8674578840,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-hydroxyphenyldimethylsulfomethyl sulfate 2.66 g (0.01 mol) was heated and dissolved in 40 ml of acetonitrile. Oleic acid 2.82 g (0.01 mol) was added to the solution obtained, and the mixture was stirred at 0° C. To the mixture solution, dicyclohexyl carbodiimide 2.06 g (0.01 mol) was added little by little, and the solution was stirred for 2 hours at 0° C. and then for 2 hours at room temperature. The solution reacted was filtered to remove dicyclohexyl urea, and the filtrate was distilled in vacuo to obtain oily residue. D-serine 1.05 g (0.01 mol) and triethyl amine 1.4 ml (0.01 mol) were added to 10 ml of water. An acetonitrile solution of the above oily residue was added to the mixture with stirring, and stirred for 10 hours at room temperature. After reaction, the reaction mixture was concentrated under reduced pressure. The concentrate was adjusted to pH 2 or 3 with 6N-HCl, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous sodium acetate, and freed of solvent in vacuo. The oily residue obtained was purified by column chromatography (column: 2.5×15 cm) on 50 g of silica gel and N-oleoyl-D-serine 1.5 g was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05112863
Quelldatensatzuspto-grants-1992_05
ORD IDord-591aa5c240de4bb69a7ae1a87f3afa6d
Quellennotizuspto-grants-1992_05