Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Glufosinate → HCID 178476818, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Glufosinate | HCID 4794 | — |
| 반응물 | Ethylene | HCID 6325 | — |
| 반응물 | Phosphorus trichloride | HCID 24387 | — |
| 반응물 | Aluminum tetrachloride | HCID 25114082 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | HCID 178476818 | HCID 178476818 | — |
반응 단계
Alternatively, another method of producing glufosinate generally comprises converting phosphorus trichloride to an adduct of methylphosphonous trichloride and aluminum tetrachloride (i.e., CH3PCl3.AlCl4). The adduct may be reacted with ethylene to form an intermediate adduct, which then may be reacted with ethanol to form ethyl 1-(2-chloroethyl)-methylphosphinate. Ethyl 1-(2-chlroethyl)-methylphosphinate may then be reacted with potassium hydroxide and ethanol to prepare the requisite ethyl vinylphosphinate precursor. The ethyl vinylphosphinate precursor is subjected to hydroformylation-aminocarbonylation, followed by hydrolysis of the hydroformylation-aminocarbonylation product in the presence of hydrochloric acid to produce glufosinate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09394173B2 |
| 출처 데이터셋 | uspto-grants-2016_07 |
| ORD ID | ord-b89d5643e0f34372973f9ff0beb82117 |
| 출처 메모 | uspto-grants-2016_07 |