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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 968044생성일: 2026년 10월 25일

Acrylic Acid → N-Propylacetamide

https://huagongshe.com/reaction/968044

반응식

참여 물질

역할이름HCID투입량
반응물Acrylic AcidHCID 6581—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물2-Amino-2-hydroxybutanoic acidHCID 18461115—
용매WaterHCID 962—
생성물N-PropylacetamideHCID 21407—
생성물N-(n-Propyl) acrylamideHCID 114794—

반응 단계

Acrylic acid (20 g) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (30 g) were dissolved in water (300 mL). Then aminohydroxybutyric acid (2.0 g) was added to the obtained solution and reacted at room temperature for 10 hours. After the completion of the reaction, water was distilled off and the residue was sufficiently washed with hexane (200 mL) in 3 portions. Next, this residue was dissolved in dimethyl-formamide (350 mL), in which N-hydroxysuccinimide (3 g) and N,N′-dicyclohexylcarbodiimide (3 g) had been dissolved, and reacted overnight. After the completion of the reaction, the solvent was distilled off. Ethyl acetate was added to the residue thus obtained and the precipitate thus formed was filtered off. The filtrate was recovered and a fraction containing the target product was taken up by silica gel column chromatography with the use of ethyl acetate as a mobile phase and alumina column chromatography. Next, a half of the solvent was distilled off with an evaporator and recrystallization was carried out by adding a hexane solvent at −20° C. to thereby give the target monomers (N-propylacetamide, N-propyl acrylamide) (yield: 68%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06956077B1
출처 데이터셋uspto-grants-2005_10
ORD IDord-33f6db3f89e74ea7acae4abe5a8385b0
출처 메모uspto-grants-2005_10