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HRID 614670作成日:2026年10月25日

Acetic Acid → N-(1,1-Dimethyl-3-oxobutyl)-2-diethylphosphonoacrylamide

https://huagongshe.com/reaction/614670

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Diethyl (3-oxobutyl)phosphonateHCID 14033—
反応物DiethylphosphiteHCID 3780918—
反応物SodiumHCID 5360545—
反応物4-Acrylamido-4-methyl-2-pentanoneHCID 21584921—
溶媒EthanolHCID 702—
生成物N-(1,1-Dimethyl-3-oxobutyl)-2-diethylphosphonoacrylamideHCID 2132824797%

反応手順

Using the same procedure of Example 1 for the preparation of diethyl 3-oxobutylphosphonate, a solution prepared from the reaction of 3.1 grams (0.135 mole) of sodium with 63 ml of anhydrous ethanol was added under nitrogen and drying conditions with stirring at room temperature to 152 grams (1 mole) of diethyl phosphite. To this solution was then added over a one hour period maintaining the internal temperature at 30°-40° C. with external cooling, 169 grams (1 mole) of diacetone acrylamide. The solution was then stirred for another hour at 24° C. before 8.2 grams (0.135 mole) of acetic acid was slowly added to bring the pH to 5. The solution was dried at 70° C./16 mm and topped off by distillation for 30 minutes with a maximum pot temperature of 120° C. at 0.2 mm. The pot residue (316 grams) was the desired N-(1,1-dimethyl-3-oxybutyl)-2-diethylphosphonoacrylamide in a 97% yield. Structure of the desired product with a purity of about 95% was confirmed by NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04145510
出典データセットuspto-grants-1979_03
ORD IDord-1831c8b74e5a468eb10f888031e8b840
出典メモuspto-grants-1979_03