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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822250Generated: October 26, 2026

Cesium carbonate → 1-(3-Bromo-phenoxy)-4-chloro-2-phenoxy-benzene

https://huagongshe.com/reaction/1822250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBenzene, 1-bromo-3-iodo-HCID 11561—
Reactant2,2,6,6-Tetramethyl-3,5-heptanedioneHCID 70700—
Reactant4-Chloro-2-phenoxyphenolHCID 12774295—
CatalystCuprous chlorideHCID 62652—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(3-Bromo-phenoxy)-4-chloro-2-phenoxy-benzeneHCID 5789422740.1%

Reaction Steps

A solution of 4-chloro-2-phenoxy-phenol (1.65 g, 7.5 mmol), 1-bromo-3-iodobenzene (6.35 g, 22.4 mmol), copper(I) chloride (0.37 g, 3.74 mmol), 2,2,6,6-tetramethyl-3,5-heptanedione (0.345 g, 1.87 mmol), and cesium carbonate (2.93 g, 9 mmol) in NMP (20 mL) is heated to 120° C. The reaction is stirred overnight and cooled to rt. The reaction is quenched with 1N aqueous HCL and extracted with ethyl ether. The organic is washed with brine, dried over sodium sulfate, filtered, and the solvent is removed. The crude is purified by silica gel column chromatography using 5/1 hexanes/ethyl acetate to elute the pure product. The solvent is removed to afford 1.13 g (40%) of the desired product. 1H NMR (400 MHz, CDCl3); MS (ES+) m/z mass calculated for C18H12BrClO2 374, found 375 and 377 (M+1 and M+3, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608639B2
Source datasetuspto-grants-2009_10
ORD IDord-1c85522644d042b78eaa5e86f3f6c207
Source noteuspto-grants-2009_10