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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875145Generated: October 27, 2026

1-Bromo-3-chloro-5-fluorobenzene → 2-[(3-Bromo-5-chlorophenyl)oxy]-1-chloro-3-fluoro-4-methylbenzene

https://huagongshe.com/reaction/1875145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloro-5-fluorobenzeneHCID 2736223—
Reactant6-Chloro-2-fluoro-3-methylphenolHCID 2773684—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product2-[(3-Bromo-5-chlorophenyl)oxy]-1-chloro-3-fluoro-4-methylbenzeneHCID 6848661557.2%

Reaction Steps

To a solution of 6-chloro-2-fluoro-3-methylphenol (7.67 g, 47.7 mmol) in DMSO (100 ml) was added potassium t-butoxide (1.0 M solution in THF) (50.1 ml, 50.1 mmol) and the mixture was stirred at room temperature for 30 minutes. Next, 1-bromo-3-chloro-5-fluorobenzene (10.0 g, 47.7 mmol) was added and the mixture was heated at 135° C. for 3 days. The reaction mixture was cooled to room temperature, diluted with EtOAc and washed with water. The solvent was removed to give 2-[(3-bromo-5-chlorophenyl)oxy]-1-chloro-3-fluoro-4-methylbenzene (9.54 g, 27.3 mmol, 57% yield) which was used in the next step without further purification. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.44 (s, 1H), 7.33-7.40 (m, 1H), 7.27 (t, 1H), 7.07 (s, 1H), 6.95-7.02 (m, 1H), 2.23 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-22a94a675c3941e391d2068a221ad20c
Source noteuspto-grants-2012_11