HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dichlorophenol → Benzene, 1,2-dichloro-4-(4-((trifluoromethyl)sulfonyl)phenoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dichlorophenol | HCID 7258 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Chloro-4-(trifluoromethylsulfonyl)benzene | HCID 703324 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Benzene, 1,2-dichloro-4-(4-((trifluoromethyl)sulfonyl)phenoxy)- | HCID 514861 | 86.3% |
Reaction Conditions
| Temperature | 125 °C |
|---|
Reaction Steps
To a solution of 4.7 g (0.0192 mole) of 4-chlorophenyl trifluoromethyl sulfone prepared according to known procedures (see E. A. Nodiff et al., J. Org. Chem., 25, 60 (1959)) and 4.7 g (0.0288 mole) of 3,4-dichlorophenol dissolved in 150 ml of DMSO was added 4.0 g (0.0288 mole) of K2CO3. The reaction mixture was heated at 125° C. for 3.5 hrs and the product recovered (6.15 g, 86.3% yield) as described in Example 18. Recrystallization from ethanol afforded purified 4-(4-((trifluoromethyl)sulfonyl)phenoxy)-1,2-dichlorobenzene, mp 77°-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04349568 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-0e6f662f7af64678a38eb9f1fabd23af |
| Source note | uspto-grants-1982_09 |