HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629847Generated: November 1, 2026
Formaldehyde → N-(Carboxymethyl)-N-(phosphonomethyl)glycine
https://huagongshe.com/reaction/629847
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Iminodiacetic acid | HCID 8897 | — |
| Reactant | Phosphorous acid | HCID 107909 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(Carboxymethyl)-N-(phosphonomethyl)glycine | HCID 80092 | 79.5% |
Reaction Steps
In a three-necked round-bottom flask equipped with a mechanical stirrer, 33.28 g (0.25 mol) of iminodiacetic acid (IDA) were mixed with 20.5 g (0.25 mol, 1 eq.) of phosphorous acid, 122.5 g (1.25 mol, 5 eq.) of phosphoric acid and 13.6 g of water. The reaction mixture was heated to 130° C. 18.80 ml of 36.6 wt.-% aqueous solution of formaldehyde (1 eq.) were then added over 118 min. During the addition, the temperature of the reaction mixture decreased from 130° C. to 124° C. At the end of the formaldehyde addition the reaction mixture was kept at reflux for 30 min. The precipitate formed by cooling the reaction mixture was isolated by filtration and washed with fresh water. After drying precipitate was analysed by H and 31P NMR and identified as 94.4% pure N-(phosphonomethyl)iminodiacetic acid (PMIDA, 39.7 g, 79.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315528B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-16104a91b1a547de9437b515e079a667 |
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| Source note | uspto-grants-2016_04 |
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