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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359204Generated: November 2, 2026

Potassium Hydroxide → 5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene

https://huagongshe.com/reaction/2359204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantBromodifluoromethyl diethylphosphonateHCID 144101—
Reactant4-Bromo-2,6-dimethoxyphenolHCID 14845876—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzeneHCID 5843207162%

Reaction Conditions

Temperature-78 °C

Reaction Steps

5-Bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene was synthesized from 4-bromo-2,6-dimethoxyphenol according to the procedure of Zafrani, Y. Tetrahedron 2009, 65, 5278 as follows. To a solution of 4-bromo-2,6-dimethoxyphenol (1.08 g, 4.6 mmol) in MeCN (27 mL) was added a solution of KOH (5.0 g, 89 mmol) in H2O (27 mL). The mixture was immediately cooled over a −78° C. bath and diethyl(bromodifluoromethyl)phosphonate (1.6 mL, 8.9 mmol) was added. The flask was sealed with a septum and the cold bath was removed. The mixture was stirred for a total of 3.5 hrs during which time the septum was ejected from the flask. The reaction was diluted with EtOAc and the layers were separated. The aqueous layer was extracted with EtOAc and the combined organics were washed with 1 M NaOH, H2O and brine then dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (0-30% EtOAc-hexanes) provided 5-bromo-2-(difluoromethoxy)-1,3-dimethoxybenzene as a white solid (0.808 g, 62% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685975B2
Source datasetuspto-grants-2014_04
ORD IDord-d7050151ffef451383eb5dfa0e487750
Source noteuspto-grants-2014_04