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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053534Generated: October 25, 2026

Glufosinate → HCID 178476818, compound

https://huagongshe.com/reaction/1053534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlufosinateHCID 4794—
ReactantEthyleneHCID 6325—
ReactantPhosphorus trichlorideHCID 24387—
ReactantAluminum tetrachlorideHCID 25114082—
SolventEthanolHCID 702—
ProductHCID 178476818HCID 178476818—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394173B2
Source datasetuspto-grants-2016_07
ORD IDord-b89d5643e0f34372973f9ff0beb82117
Source noteuspto-grants-2016_07