Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Phosphorus trioxide | HCID 14810 | — |
| Edukt | N-(hydroxymethyl)benzamide | HCID 80493 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Benzoylaminomethanephosphonic acid | HCID 10443251 | — |
Reaktionsschritte
50 ml of acetic acid were cooled to 10° C. with stirring and under a nitrogen atmosphere. 11 g (0.1 mol) of diphosphorus trioxide (P2O3) were then added dropwise with further cooling, during the course of which the temperature fell to 0° to 5° C. 30.2 g (0.2 mol) of N-hydroxymethylbenzamide were then added in portions at 5°-10° C. during the course of 60 minutes. The mixture was then stirred without cooling until room temperature was reached. It was then heated to reflux for 31/2 hours. It was then cooled. 2 g (0.11 mol) of water were then added dropwise with stirring, the temperature rising to 35° C. The mixture was then allowed to cool and 25 ml of acetone were added. It was then additionally stirred and filtered with suction. 31.5 g of benzoylaminomethanephosphonic acid having a melting point of 165° to 170° C. were obtained. A further 2 g were isolated from the mother liquor. Altogether, 33.5 g (78% of theory) were thus obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05155257 |
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| Quelldatensatz | uspto-grants-1992_10 |
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| ORD ID | ord-bc284abc92c947ff8bed53243a736aa5 |
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| Quellennotiz | uspto-grants-1992_10 |
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