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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260571Generated: October 26, 2026

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

https://huagongshe.com/reaction/260571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSulfuric AcidHCID 1118—
ReactantIminodiacetic acidHCID 8897—
ReactantPhosphorous acidHCID 107909—
ProductN-(Carboxymethyl)-N-(phosphonomethyl)glycineHCID 8009295.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527953
Source datasetuspto-grants-1996_06
ORD IDord-10b21984e73a43a1a748890a86a19b27
Source noteuspto-grants-1996_06