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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 278524생성일: 2026년 10월 26일

Acetic Acid → HCID 178511211, 화합물

https://huagongshe.com/reaction/278524

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물AcroleinHCID 7847—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium CyanideHCID 8929—
반응물Diethyl methylphosphonateHCID 12685—
반응물Ammonium ChlorideHCID 25517—
용매AmmoniaHCID 222—
용매EthanolHCID 702—
생성물HCID 178511211HCID 178511211—

반응 조건

온도30 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06359162B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-b0e01c018bd44298af318637fdb4df3f
출처 메모uspto-grants-2002_03