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HRID 278523作成日:2026年10月26日

Acetic Acid → HCID 178511211、化合物

https://huagongshe.com/reaction/278523

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrochloric AcidHCID 313—
反応物AcroleinHCID 7847—
反応物Acetic AnhydrideHCID 7918—
反応物Sodium CyanideHCID 8929—
反応物Diethyl methylphosphonateHCID 12685—
反応物Ammonium ChlorideHCID 25517—
溶媒AmmoniaHCID 222—
溶媒EthanolHCID 702—
生成物HCID 178511211HCID 178511211—

反応条件

温度30 °C

反応手順

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 25-30° C., 13.61 g (0.10 mol) of diethyl methanephosphonate are subsequently added dropwise. The mixture is stirred at 30° C. for 2 hours and then, at 25-28° 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 19.4 g (98% of theory) of 2-amino-4-(hydroxymethylphosphinyl)butyric acid, ammonium salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06359162B1
出典データセットuspto-grants-2002_03
ORD IDord-22ecc69999914860b72ae2adbe0cf395
出典メモuspto-grants-2002_03