HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Carfentrazone-ethyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Carfentrazone | HCID 443229 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Carfentrazone-ethyl | HCID 86222 | 91% |
Reaction Steps
To a flask was added 140 g of the 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propionic acid, obtained according to the Example 4, 70 g of ethanol, 1.8 g of a concentrated sulfuric acid and 500 g of methyl benzene. The mixture was refluxed for 15 hours to react. The excess ethanol was recovered by distillation. At room temperature the mixture was washed with 200 g of water, with 200 g of a 6% (wt/wt) aqueous solution of sodium carbonate and finally with water. The solvent was completely removed under reduced pressure to give carfentrazone-ethyl as a faint yellow transparent and viscous liquid in a yield of 91% with a purity of 98.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957220B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-6b6d7b10fcbc4c35bee9c05dc9d4b67a |
| Source note | uspto-grants-2015_02 |