Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Acrolein | HCID 7847 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Sodium Cyanide | HCID 8929 | — |
| Edukt | Diethyl methylphosphonate | HCID 12685 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Lösungsmittel | Ammonia | HCID 222 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 178511211 | HCID 178511211 | — |
Reaktionsschritte
At room temperature, 5.61 g (0.10 mol) of freshly distilled acrolein are added to 10.21 g (0.10 mol) of acetic anhydride. At 25 to 30° C., this mixture is subsequently added dropwise to 13.61 g (0.10 mol) of diethyl methanephosphonate and 4.6 g (0.1 mol) of ethanol. The mixture is stirred at 30° C. for 2 hours and then, at 25 to 28° C., added dropwise to a solution of 4.9 g (0.10 mol) of sodium cyanide and 10.7 g (0.20 mol) of ammonium chloride in 50 ml of ammonia (25% strength). After 2 hours at 30° C., the crude aminonitrile is added dropwise to 200 ml of hydrochloric acid (37% strength). The mixture is subsequently heated under reflux for 2 hours, while ethanol and acetic acid are distilled off. The mixture is concentrated using a rotary evaporator, a pH of approximately 9 is set using ammonia solution and the product is purified by crystallization from methanol. This gives 19.6 g (99% of theory) of 2-amino-4-(hydroxymethylphosphinyl)-butyric acid, ammonium salt.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06359162B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-b0e01c018bd44298af318637fdb4df3f |
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| Quellennotiz | uspto-grants-2002_03 |
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