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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260571생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/260571

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sulfuric AcidHCID 1118—
반응물Iminodiacetic acidHCID 8897—
반응물Phosphorous acidHCID 107909—
생성물N-(Carboxymethyl)-N-(phosphonomethyl)glycineHCID 8009295.9%

반응 조건

온도120 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05527953
출처 데이터셋uspto-grants-1996_06
ORD IDord-10b21984e73a43a1a748890a86a19b27
출처 메모uspto-grants-1996_06