HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene → HCID 178476818, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Phosphinothricin | HCID 91619 | — |
| Reactant | Aluminum tetrachloride | HCID 25114082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178476818 | HCID 178476818 | — |
Reaction Steps
Another process of producing phosphinothricin generally comprises converting phosphorus trichloride to an adduct of methylphosphonous trichloride and aluminum tetrachloride (i.e., CH3PCl3.AlCl4). The adduct is reacted with ethylene to form an intermediate adduct, which is then reacted with ethanol to form ethyl 1-(2-chloroethyl)-methylphosphinate. This compound is reacted with potassium hydroxide and ethanol to prepare an 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 phosphinothricin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981142B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-402523d6d8d74830b45d44bbad92c16d |
| Source note | uspto-grants-2015_03 |