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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094823Generated: November 1, 2026

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

https://huagongshe.com/reaction/1094823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 2-chloro-, 1-(4-methylbenzenesulfonate)HCID 6639—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-fluorophenolHCID 605472—
SolventDimethylformamideHCID 6228—
SolventSodium HydroxideHCID 14798—
Product2-Bromo-1-(2-chloroethoxy)-4-fluorobenzeneHCID 4313560250%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of toluene-4-sulfonic acid 2-chloroethyl ester (2.80 g, 11.93 mmol) in anhydrous N,N-dimethylformamide (10 ml) was added 2-bromo-4-fluorophenol (2.73 g, 14.30 mmol), and potassium carbonate (3.30 g, 23.90 mmol). The resulting solution was then heated at 50° C. with stirring for 6 hours. After cooling to room temperature, the reaction mixture was diluted with sodium hydroxide (1M aqueous solution, 30 ml) and tert-butyldimethyl ether (50 ml) was added. The layers were separated and the organic extract was washed with saturated brine solution (30 ml), prior to being dried over anhydrous MgSO4 (s), filtered and evaporated in vacuo. Purification by column chromatography eluting with ethyl acetate:heptane 1:99 to 10:90 afforded the title compound as a colourless oil (1.50 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134007B2
Source datasetuspto-grants-2012_03
ORD IDord-a1156f02ed1748ab858b7816fc1a6c15
Source noteuspto-grants-2012_03