戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 260571作成日:2026年10月26日

Formaldehyde → N-(Carboxymethyl)-N-(phosphonomethyl)glycine

https://huagongshe.com/reaction/260571

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sulfuric AcidHCID 1118—
反応物Iminodiacetic acidHCID 8897—
反応物Phosphorous acidHCID 107909—
生成物N-(Carboxymethyl)-N-(phosphonomethyl)glycineHCID 8009295.9%

反応条件

温度120 °C

反応手順

Concentrated filtrates from Cycle 1 were charged to a 500 ml three neck flask fitted with thermometer, condenser, dropping funnel and stirrer. Phosphorous acid (40.8 g, 0.493 moles), iminodiacetic acid (63.6 g, 0.469 moles) and sulphuric acid (5.0 g, 0.050 moles) were added, with stirrring, to the flask (sulphuric acid was charged on the assumption that 10% of the sulphuric acid was lost in the wash and filter cake). The reaction mixture was then heated to 120° C. and formaldehyde (46.1 g at 36.1% strength, 0.555 moles) was then added over one hour. The temperature was maintained between 110° and 120° C. during addition. On complete addition the reaction mixture was allowed to cool to 25° C. over 90 minutes. The reaction mixture was filtered and the filter cake washed with water (57 ml). The product was dried in a vacuum oven to yield 102.2 g of N-phosphonomethyliminodiacetic acid at 95.4% strength equivalent to a cumulative isolated yield of 75.3%. The filtrates (99.3 g) and the water wash (76.8 g) were analysed at 7.5% and 3.7% N-phosphonomethyliminodiacetic acid respectively. This was equivalent to a total cumulative conversion yield of 81.7% N-phosphonomethyliminodiacetic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05527953
出典データセットuspto-grants-1996_06
ORD IDord-10b21984e73a43a1a748890a86a19b27
出典メモuspto-grants-1996_06