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HRID 483067作成日:2026年10月26日

Formaldehyde → [(2,4-Dioxoimidazolidin-1-yl)methyl]phosphonic acid

https://huagongshe.com/reaction/483067

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Acetic AnhydrideHCID 7918—
反応物HydantoinHCID 10006—
反応物Phosphorous acidHCID 107909—
溶媒Acetic AcidHCID 176—
生成物[(2,4-Dioxoimidazolidin-1-yl)methyl]phosphonic acidHCID 13605838110.3%

反応手順

A 500 ml round-bottom flask was equipped with a thermometer, condenser, magnetic stirrer, and heating mantle. Into the flask was charged, under nitrogen, 10.0 g (0.100 mole) of hydantoin, 3.2 g (0.10 mole) of paraformaldehyde (purity: ca 95%), and 60 ml of anhydrous acetic acid. The resulting mixture was heated at reflux for 0.75 hour and then cooled. To the resulting clear solution was added 8.5 g (0.100 mole) of 97% phosphorous acid and 30.6 g (0.300 mole) of acetic anhydride. The reaction mixture was heated to reflux over 1.2 hours and held at reflux for another 0.1 hour. (A white solid precipitated early in the heating period and then redissolved toward the end.) The reaction mixture was cooled somewhat, and 150 ml of water was added to it. The resulting solution was heated at reflux for 2.0 hours, cooled, and vacuum stripped at 70° C. to give 21.4 g of crude 1-(phosphonomethyl)hydantoin as an oil. Quantitative analysis by hplc showed the yield of 1-(phosphonomethyl) hydantoin to be 46%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04578224
出典データセットuspto-grants-1986_03
ORD IDord-6033f85baadb4db3b3c61a3567442dd2
出典メモuspto-grants-1986_03