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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64925생성일: 2026년 10월 24일

Triethylamine → 2-[beta-(2-furyl)acrylamido]-N5-methyl-N1,N1-di(n-propyl)pentane-1,5-diamide

https://huagongshe.com/ko/reaction/64925

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Furylacrylic acidHCID 10876—
반응물Ethyl chloroformateHCID 10928—
반응물HCID 86740989HCID 86740989—
용매DichloromethaneHCID 6344—
생성물2-[beta-(2-furyl)acrylamido]-N5-methyl-N1,N1-di(n-propyl)pentane-1,5-diamideHCID 8674099080%

반응 단계

In 75 ml of methylene chloride was dissolved 1.5 g of β-(2-furyl)acrylic acid, and 2.7 g of triethylamine and 1.3 g of ethyl chlorocarbonate were successively added thereto dropwise at -25° C. to -20° C. After 30 minutes, 3 g of the DL-2-amino-N5 -methyl-N1,N1 -di(n-propyl)-pentane-1,5-diamide hydrochloride was added to the above solution, and the resulting mixture was subjected to reaction at the same temperature for 30 minutes and at room temperature for 30 minutes. After completion of the reaction, the reaction mixture was washed successively with 30 ml of a 5% aqueous sodium hydroxide solution, 30 ml of diluted hydrochloric acid and 30 ml of water and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure to obtain 3.1 g (yield 80%) of DL-2-[β-(2-furyl)acrylamido]-N5 -methyl-N1,N1 -di(n-propyl)pentane-1,5-diamide having a melting point of 112°-113° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04610983
출처 데이터셋uspto-grants-1986_09
ORD IDord-47a1a8fa8c3e452ea1b4ee37c4296f87
출처 메모uspto-grants-1986_09