Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 260572Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/260572

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktSulfuric AcidHCID 1118—
EduktIminodiacetic acidHCID 8897—
EduktPhosphorous acidHCID 107909—
ProduktN-(Carboxymethyl)-N-(phosphonomethyl)glycineHCID 8009288,4%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Concentrated filtrates from reaction 2 was charged to a 250 ml three neck flask fitted with thermometer, condenser, dropping funnel and stirrer. Phosphorous acid (39.1 g, 0.472 moles), iminodiacetic acid (60.9 g, 0.449 moles) and sulphuric acid (4.79 g, 0.0479 moles) were added, with stirring, to the flask. The reaction mixture was then heated to 120° C. and formaldehyde (44.2 g at 36.1% strength, 0.533 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 90.1 g of N-phosphonomethyliminodiacetic acid at 95.6% strength equivalent to a cumulative isolated yield of 78.2%. The filtrates (91.1 g) and the water wash (71.8 g) were analysed at 5.0% and 3.0% N-phosphonomethylimiodiacetic acid respectively. This was equivalent to a total cumulative conversion yield of 82.3% N-phosphonomethyliminodiacetic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05527953
Quelldatensatzuspto-grants-1996_06
ORD IDord-495b62f4907c44fc81c8d2a5d0797a3f
Quellennotizuspto-grants-1996_06