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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1053534생성일: 2026년 10월 27일

Glufosinate → HCID 178476818, 화합물

https://huagongshe.com/reaction/1053534

반응식

참여 물질

역할이름HCID투입량
반응물GlufosinateHCID 4794—
반응물EthyleneHCID 6325—
반응물Phosphorus trichlorideHCID 24387—
반응물Aluminum tetrachlorideHCID 25114082—
용매EthanolHCID 702—
생성물HCID 178476818HCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394173B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-b89d5643e0f34372973f9ff0beb82117
출처 메모uspto-grants-2016_07