돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34554생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/34554

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acidHCID 128570—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-ethanolamineHCID 5425340794%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762829
출처 데이터셋uspto-grants-1988_08
ORD IDord-99e504bb448c4305b358b316d51c7e72
출처 메모uspto-grants-1988_08