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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278524Generated: October 25, 2026

Acetic Acid → HCID 178511211, compound

https://huagongshe.com/reaction/278524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantAcroleinHCID 7847—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium CyanideHCID 8929—
ReactantDiethyl methylphosphonateHCID 12685—
ReactantAmmonium ChlorideHCID 25517—
SolventAmmoniaHCID 222—
SolventEthanolHCID 702—
ProductHCID 178511211HCID 178511211—

Reaction Conditions

Temperature30 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359162B1
Source datasetuspto-grants-2002_03
ORD IDord-b0e01c018bd44298af318637fdb4df3f
Source noteuspto-grants-2002_03