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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355376Generated: October 31, 2026

2-Bromophenol → 1-Bromo-2-(3-fluorophenoxy)benzene

https://huagongshe.com/reaction/2355376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantTriethylamineHCID 8471—
Reactant3-Fluorophenylboronic acidHCID 2733986—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product1-Bromo-2-(3-fluorophenoxy)benzeneHCID 1842351048%

Reaction Steps

To a stirred solution of 3-fluorophenylboronic acid (2.10 g, 15 mmol), 2-bromophenol (1.77 g, 10 mmol) and Cu(OAc)2 (0.93 g, 5 mmol) in anhydrous CH2Cl2 (25 mL) was added activated 4 Å molecular sieves (˜0.1 g), followed by anhydrous Et3N (3.5 mL, 25 mmol). The resulting dark green solution was stirred at rt for 48 h. The mixture was evaporated under reduced pressure and the residue was washed several times with Et2O (˜150 mL). The Et2O solution was washed with sat'd aq NH4Cl, and 1 N aq HCl. The organic layer was evaporated and the crude product was purified by flash column chromatography to give 1-(3-fluorophenoxy)-2-bromobenzene (1.28 g, 48%) as clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-4494bae283b74c4f9ca75b71df71b56d
Source noteuspto-grants-2010_07