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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851631Generated: November 2, 2026

4-Bromophenol → 2-(4-Bromophenoxy)-5-methoxybenzoic acid

https://huagongshe.com/reaction/1851631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-methoxybenzoic acidHCID 89906—
SolventTolueneHCID 1140—
Product2-(4-Bromophenoxy)-5-methoxybenzoic acidHCID 57475632—

Reaction Steps

A RBF equipped with a reflux condenser was charged with 2-bromo-5-methoxy benzoic acid (430 g, 1.8614 mol), 4-bromo phenol (322 g, 1.8614 mol, 1 eq), potassium carbonate (514.5 g, 3.7 228 mol, 2.0 eq) and CuOTf-toluene complex (24.08 g, 0.04653 mol, 0.025 eq). Ethyl acetate (9.0 ml 0.09679 mol, 0.052) and toluene (1.3 L) was carefully added portion wise. After stirring at RT for 10 min, the mixture was heated to 50° C. and stirred for 30 min. The mixture was then heated to 110° C. for 20 hrs. The reaction was monitored by TLC. After 20 hrs, TLC showed total consumption of starting materials. The reaction mixture was cooled to RT, diluted with water and acidified by 2N HCl. The reaction mixture was extracted with ethyl acetate (3.0×2 liter) followed by filteration of the extract through celite bed and washing with ethyl acetate (1.0 liter). Combined extracts were dried over sodium sulfate and concentrated to yield a crude mass of 590 g. (Dark brown solid). This mass was used directly in step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957083B2
Source datasetuspto-grants-2015_02
ORD IDord-fd146bc4dee84d3794b6b89f0e633711
Source noteuspto-grants-2015_02