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HRID 968044作成日:2026年10月26日

Acrylic Acid → N-Propylacetamide

https://huagongshe.com/reaction/968044

反応式

関与物質

役割名称HCID仕込み量
反応物Acrylic AcidHCID 6581—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2-Amino-2-hydroxybutanoic acidHCID 18461115—
溶媒WaterHCID 962—
生成物N-PropylacetamideHCID 21407—
生成物N-(n-Propyl) acrylamideHCID 114794—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06956077B1
出典データセットuspto-grants-2005_10
ORD IDord-33f6db3f89e74ea7acae4abe5a8385b0
出典メモuspto-grants-2005_10