戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 34554作成日:2026年10月27日

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

https://huagongshe.com/reaction/34554

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acidHCID 128570—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-ethanolamineHCID 5425340794%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04762829
出典データセットuspto-grants-1988_08
ORD IDord-99e504bb448c4305b358b316d51c7e72
出典メモuspto-grants-1988_08