HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-chloro-N-(2,6-diiodo-4-(perfluoropropan-2-yl)phenyl)-3-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloro-3-nitrobenzoyl chloride | HCID 12627413 | — |
| Reactant | 2,6-Diiodo-4-(perfluoropropan-2-yl)aniline | HCID 58297549 | — |
| Solvent | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Product | 2-chloro-N-(2,6-diiodo-4-(perfluoropropan-2-yl)phenyl)-3-nitrobenzamide | HCID 86654243 | 103.5% |
Reaction Conditions
| Temperature | 135 °C |
|---|
Reaction Steps
To a solution of 40.0 g (78.0 mmol) of 2,6-diiodo-4-(perfluoropropan-2-yl)aniline in 100 ml of DMI was added 20.6 g (94.0 mmol) of 2-chloro-3-nitrobenzoyl chloride, followed by stirring at 135° C. for 3 hours. After cooling to room temperature, the reaction mixture was poured into 1000 ml of water. After extraction with the addition of 1000 ml of ethyl acetate, the organic layer was washed with water and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was washed with hexane to prepare 56.2 g (yield 99%) of a target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08686044B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-92f7d1d943aa47c7890a8e99e0e3ca68 |
| Source note | uspto-grants-2014_04 |