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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260570Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/260570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktWaterHCID 962—
EduktSulfuric AcidHCID 1118—
EduktIminodiacetic acidHCID 8897—
EduktPhosphorous acidHCID 107909—
ProduktN-(Carboxymethyl)-N-(phosphonomethyl)glycineHCID 8009261%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Water (17.3 g, 0.961 moles) was charged to a 250 ml three neck flask fitted with thermometer, condenser, dropping funnel and stirrer. Phosphorous acid (42.6 g, 0.514 moles), sulphuric acid (50.0 g, 0.500 moles--added over 10 minutes during which an exotherm from 20° C. to 60° C. was observed) and iminodiacetic acid (66.5 g,0.490 moles) were added to the stirred reaction flask. The reaction mixture was then heated to 120° C. and formaldehyde (48.2 g at 36.1% strength, 0.580 moles) was 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 and the reaction mixture was filtered. The filter cake was washed with water (57 ml) and the product was dried in a vacuum oven to yield 67.9 g of N-phosphonomethyliminodiacetic acid at 98.0% strength, equivalent to an isolated yield of 59.8%. The filtrates (128.0 g) and the water wash (66.0 g) were analysed at 13.7% and 5.5% N-phosphonomethyliminodiacetic acid respectively. This was equivalent to a total conversion yield of 78.9% N-phosphonomethyliminodiacetic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05527953
Quelldatensatzuspto-grants-1996_06
ORD IDord-881c40ec38ba494984efd934042e0713
Quellennotizuspto-grants-1996_06