HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-fluoro-4-nitrobenzoate → Methyl 3-[[3-chloro-4-(trifluoromethoxy)phenyl]amino]-4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-fluoro-4-nitrobenzoate | HCID 592761 | — |
| Reactant | 3-Chloro-4-(trifluoromethoxy)aniline | HCID 2773843 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-[[3-chloro-4-(trifluoromethoxy)phenyl]amino]-4-nitrobenzoate | HCID 68662839 | 38% |
Reaction Steps
A solution of methyl 3-fluoro-4-nitrobenzoate (1.99 g, 10 mmol) and 3-chloro-4-(trifluoromethoxy)aniline (4.23 g, 20 mmol) in dimethylsulfoxide (10 mL) was stirred at 160° C. for 2 days. After cooling, the reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1) and recrystallized from hexane/ethyl acetate to give the title compound (1.47 g, yield 38%) as orange crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492378B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-e627c0574fc34a9d829d9a8702b2a97b |
| Source note | uspto-grants-2013_07 |