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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278524Erstellt: 25. Oktober 2026

Acetic Acid → HCID 178511211, Verbindung

https://huagongshe.com/reaction/278524

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
EduktAcroleinHCID 7847—
EduktAcetic AnhydrideHCID 7918—
EduktSodium CyanideHCID 8929—
EduktDiethyl methylphosphonateHCID 12685—
EduktAmmonium ChlorideHCID 25517—
LösungsmittelAmmoniaHCID 222—
LösungsmittelEthanolHCID 702—
ProduktHCID 178511211HCID 178511211—

Reaktionsbedingungen

Temperatur30 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06359162B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-b0e01c018bd44298af318637fdb4df3f
Quellennotizuspto-grants-2002_03