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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831769Generated: October 31, 2026

Hydrochloric Acid → 4-Bromo-3-[2-(2,4-dichlorophenyl)-ethoxy]-5-methoxy-benzoic Acid

https://huagongshe.com/reaction/1831769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl BromideHCID 6323—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3-[2-(2,4-dichlorophenyl)ethoxy]-5-hydroxybenzoic acidHCID 22052412—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Bromo-3-[2-(2,4-dichlorophenyl)-ethoxy]-5-methoxy-benzoic AcidHCID 22052329—

Reaction Conditions

Temperature0 °C

Reaction Steps

0.2 g (0.49 mmol) of 4-Bromo-3-[2-(2,4-dichlorophenyl)-ethoxy]-5-hydroxy-benzoic acid was dissolved in 5 ml DMF and 0.272 mg (1.97 mmol) of potassium carbonate was added. The solution was cooled to 0° C. and 0.699 g (4.9 mmol) methyl bromide was added. The solution was stirred for 16 h at RT. The solvent was removed under reduced pressure. The residue was chromatographed on silica gel eluting with ethyl acetate/n-heptane (1/1). The resulting compound was dissolved in 10 ml dioxan and 1 ml water. 2N aqueous NaOH was added to the solution to give a pH of 13. The reaction solution was heated at 60° C. for 4 h. 5 ml water was added, followed by concentrated hydrochloric acid to give a pH of 1–2, whereupon the product precipitated from solution. The suspension was stirred for 30 min, then the product was filtered off and dried under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067665B2
Source datasetuspto-grants-2006_06
ORD IDord-8643b1ccb5d647a48b4a297e8e7931af
Source noteuspto-grants-2006_06