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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931550Generated: November 1, 2026

4-Bromophenol → HCID 57475643, compound

https://huagongshe.com/reaction/931550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantCesium carbonateHCID 10796—
Reactant2,5-Diiodobenzoic acidHCID 26549—
CatalystEthyl AcetateHCID 8857—
SolventTolueneHCID 1140—
ProductHCID 57475643HCID 57475643108%

Reaction Steps

A RBF equipped with a reflux condenser was charged with 4-bromophenol (15.5 g, 89.4 mmol), 2,5-diiodobenzoic acid (25.700 g, 68.7 mmol), EtOAc (0.337 ml, 3.44 mmol), and toluene (100 mL). Cs2CO3 (44.8 g, 137 mmol) was carefully added portionwise. After stirring at RT for 1 min, the mixture was heated to 50° C. for 40 min and then heated to 100° C. for 20 hrs. The reaction mixture was allowed to cool to RT. The mixture was filtered through Celite and the solids were washed with EtOAc. The filtrate was diluted with water (200 mL), acidified with 2N HCl (300 mL), and extracted with EtOAc (4×500 mL). The organic extract was washed with brine and dried over sodium sulfate. The organic fraction was concentrated under reduced pressure to afford crude 2-(4-bromophenoxy)-5-iodobenzoic acid (31.1 g) as a tan oil that solidified upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296759B2
Source datasetuspto-grants-2016_03
ORD IDord-2249ecc789124b79aeefae4725c6200d
Source noteuspto-grants-2016_03