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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702827Generated: October 25, 2026

3,4-Dichlorophenol → Benzene, 1,2-dichloro-4-(4-((trifluoromethyl)sulfonyl)phenoxy)-

https://huagongshe.com/reaction/1702827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorophenolHCID 7258—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloro-4-(trifluoromethylsulfonyl)benzeneHCID 703324—
SolventDimethyl SulfoxideHCID 679—
ProductBenzene, 1,2-dichloro-4-(4-((trifluoromethyl)sulfonyl)phenoxy)-HCID 51486186.3%

Reaction Conditions

Temperature125 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04349568
Source datasetuspto-grants-1982_09
ORD IDord-0e6f662f7af64678a38eb9f1fabd23af
Source noteuspto-grants-1982_09