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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773969Generated: November 2, 2026

Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → 4-Bromo-2-chloro-1-(2-chloroethoxy)benzene

https://huagongshe.com/reaction/1773969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 2-chloro-, 1-(4-methylbenzenesulfonate)HCID 6639—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-chlorophenolHCID 19859—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-chloro-1-(2-chloroethoxy)benzeneHCID 43135623—

Reaction Conditions

Temperature60 °C

Reaction Steps

Potassium carbonate (8.29 g, 60 mmol, 3.0 eq.) and 2-chloroethyl p-toluenesulfonate (5.16 g, 22 mmol, 1.1 eq.) were added in sequence to a solution of 4-bromo-2-chlorophenol (4.19 g, 20 mmol, 1.0 eq.) in DMF (25 mL). The resulting mixture was heated up to 60° C. and stirred at that temperature for 4 hours. The mixture was allowed to cool down to r.t. and was partitioned between AcOEt (290 mL) and water (120 mL). The layers were separated. The org. phase was washed with water (4×120 mL), dried over MgSO4, filtered, and concentrated in vacuo to give 4-bromo-2-chloro-1-(2-chloro-ethoxy)-benzene as a colorless oil that solidified upon standing. The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255090B2
Source datasetuspto-grants-2016_02
ORD IDord-e97a8e7e3c734083a67b37c694b84edd
Source noteuspto-grants-2016_02