HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glufosinate → HCID 178476818, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glufosinate | HCID 4794 | — |
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Aluminum tetrachloride | HCID 25114082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178476818 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394173B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-b89d5643e0f34372973f9ff0beb82117 |
| Source note | uspto-grants-2016_07 |