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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798613Generated: October 26, 2026

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

https://huagongshe.com/reaction/1798613

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 numberUS08343970B2
Source datasetuspto-grants-2013_01
ORD IDord-935a98956db44de6a47d9e97bd0eb71f
Source noteuspto-grants-2013_01