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HRID 22614作成日:2026年10月26日

Sodium Chloride → N-(2,2-Dimethoxyethyl)-2-propenamide

https://huagongshe.com/reaction/22614

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Acryloyl chlorideHCID 13140—
反応物Sodium HydroxideHCID 14798—
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
触媒2,2,6,6-tetramethyl-4-hydroxypiperidine-N-oxideHCID 11607999—
溶媒WaterHCID 962—
生成物N-(2,2-Dimethoxyethyl)-2-propenamideHCID 989889981.7%

反応手順

40 g (1.0 mol) of sodium hydroxide are dissolved in 100 g of water and 200 g of ice in a 1-liter reactor having a stirrer and a cooling system. The sodium hydroxide solution is cooled to 10° C., and 105.1 g (1.0 mol) of aminoacetaldehyde dimethyl-acetal and 10 mg of the inhibitor 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxide are added. 99.5 g (1.1 mol) of acrylic acid chloride are slowly added to that solution at 10° C. over a period of 2 hours. The pH value drops slowly and ultimately is adjusted to 7. According to GC, amine is no longer present. The reaction mixture is saturated with sodium chloride and extracted three times with 200 ml of tert-butyl methyl ether. The organic phase is dried, filtered and concentrated using a rotary evaporator. The resulting oil is extracted three times with petroleum ether and then dried again using a rotary evaporator. 130 g of acrylamido-acetaldehyde dimethylacetal (81% of theory) are obtained in the form of an oil; the product is 99% according to GC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849210B2
出典データセットuspto-grants-2005_02
ORD IDord-f913742319db48b68f8b62a82147532c
出典メモuspto-grants-2005_02