참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Acrolein | HCID 7847 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Sodium Cyanide | HCID 8929 | — |
| 반응물 | Diethyl methylphosphonate | HCID 12685 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 용매 | Ammonia | HCID 222 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | HCID 178511211 | HCID 178511211 | — |
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 25-30° 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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06359162B1 |
|---|
| 출처 데이터셋 | uspto-grants-2002_03 |
|---|
| ORD ID | ord-22ecc69999914860b72ae2adbe0cf395 |
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| 출처 메모 | uspto-grants-2002_03 |
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