HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384148Generated: October 25, 2026
Ethyl Acetate → 2-Chloro-1-(4-iodophenoxy)-4-(trifluoromethyl)benzene
https://huagongshe.com/reaction/384148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Iodophenol | HCID 10894 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 2-chloro-1-fluoro-4-(trifluoromethyl)- | HCID 157153 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Chloro-1-(4-iodophenoxy)-4-(trifluoromethyl)benzene | HCID 68430723 | — |
Reaction Steps
To a solution of 4-iodophenol (200 mg) in dimethylsulfoxide (1 ml), 218 mg of 2-chloro-1-fluoro-4-(trifluoromethyl)benzene and 251 mg of potassium carbonate were added, and the reaction solution was stirred at 120° C. for 3 hours. The reaction solution was cooled, ethyl acetate was added, the insoluble matter was filtered off, and the filtrate was washed with water and a saturated saline solution and dried over an anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (98:2-80/20)) to afford the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08367708B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-236a00b7ed9d4ccda644ca54e62e3c55 |
|---|
| Source note | uspto-grants-2013_02 |
|---|