Реакция #62832

Уравнение реакции

ethanolamine

triethylamine

3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoic acid

ethyl chlorocarbonate

→

title compound

Выход 94.0%

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

Выход 94.0%

Растворители

water

tetrahydrofuran

Условия реакции

Обработка

1. 1
   ТемператураWhile cooling the mixture in ice
2. 2
   workup.STIRRINGThen the mixture was stirred for 15 minutes
3. 3
   workup.STIRRINGAfter the mixture was stirred for 30 minutes at room temperature
4. 4
   Экстракцияthe resulting aqueous solution was extracted with ethyl acetate
5. 5
   ДругоеThe ethyl acetate layer was separated from the aqueous layer
6. 6
   Промывкаwashed with 5% aqueous hydrochloric acid solution
7. 7
   Сушкаwater, and dried over magnesium sulfate
8. 8
   workup.DISTILLATIONThe solvent was distilled off
9. 9
   ДругоеThe resulting reaction mixture

Методика

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.

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