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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34554Erstellt: 25. Oktober 2026

Ethanolamine → N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-ethanolamine

https://huagongshe.com/reaction/34554

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
Edukt3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acidHCID 128570—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-ethanolamineHCID 5425340794%

Reaktionsschritte

6.1 g of 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoic acid was dissolved in 50 ml of tetrahydrofuran and 3.1 ml of triethylamine was added thereto. While cooling the mixture in ice with stirring, 2.1 ml of ethyl chlorocarbonate was added dropwise. Then the mixture was stirred for 15 minutes and 1.8 ml of ethanolamine was added thereto. After the mixture was stirred for 30 minutes at room temperature, water was added thereto and the resulting aqueous solution was extracted with ethyl acetate. The ethyl acetate layer was separated from the aqueous layer, washed with 5% aqueous hydrochloric acid solution and then water, and dried over magnesium sulfate. The solvent was distilled off. The resulting reaction mixture was subjected to chromatography on a silica gel column to afford 6.5 g (yield 94%) of the title compound as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04762829
Quelldatensatzuspto-grants-1988_08
ORD IDord-99e504bb448c4305b358b316d51c7e72
Quellennotizuspto-grants-1988_08