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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325942생성일: 2026년 10월 25일

N,N'-Dicyclohexylurea → Acetyl carnitine trifluoroethyl amide

https://huagongshe.com/reaction/325942

반응식

참여 물질

역할이름HCID투입량
반응물N,N'-DicyclohexylureaHCID 4277—
반응물TriethylamineHCID 8471—
반응물2,2,2-Trifluoroethylamine hydrochlorideHCID 9772—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Acetyl carnitine chlorideHCID 131713442—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Acetyl carnitine trifluoroethyl amideHCID 131713488—

반응 단계

To a solution of 2,2,2-trifluoroethylamine hydrochloride (2.7 grams; 0.02 moles) in tetrahydrofuran (150 ml) and triethylamine (2.8 ml; 0.02 moles) was added acetyl carnitine chloride (4.8 grams; 0.02 moles) in water (10 ml) and lastly N,N'-dicyclohexylcarbodiimide (4.2 grams; 0.02 moles) dissolved in tetrahydrofuran (50 ml). The reaction mixture was kept for a whole day under stirring at room temperature. A precipitate formed. The precipitate consisting of dicyclohexyl urea was filtered and the filtrate was concentrated until complete removal of tetrahydrofuran. The residual aqueous solution was washed with CHCl3 (2×50 ml), then evaporated to dryness. The raw solid was taken up with CH3CN (30 ml), and the resulting mixture was kept at 0° C.-5° C. for 2 hours. After filtering off the unreacted acetyl carnitine, if any, upon addition of ethyl acetate-ethyl ether to the filtrate a product crystallized as a very hygroscopic solid which was stored in a nitrogen atmosphere in anhydrous conditions.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04443475
출처 데이터셋uspto-grants-1984_04
ORD IDord-cc248d42c46d49559514c0d9e927cc3f
출처 메모uspto-grants-1984_04