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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259534Generated: October 31, 2026

Hydrogen Peroxide → 3,5-Difluoro-4-difluoromethoxyphenol

https://huagongshe.com/reaction/2259534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactanttert-Butyl hydroperoxideHCID 6410—
Reactant2,6-DifluorophenolHCID 94392—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
Reactant3,5-Difluoro-4-difluoromethoxyphenolHCID 19032155—
Reactant5-Bromo-2-(difluoromethoxy)-1,3-difluorobenzeneHCID 22717514—
Product3,5-Difluoro-4-difluoromethoxyphenolHCID 19032155—
Product2-(Difluoromethoxy)-1,3-difluorobenzeneHCID 19593821—

Reaction Steps

Compound (251) can be prepared in the same manner as in Preparation Example 248, except for replacing 3-fluoro-4-difluoromethoxyphenol with 3,5-difluoro-4-difluoromethoxyphenol. The 3,5-difluoro-4-difluoromethoxyphenol can be obtained by converting 2,6-difluorophenol to a formic ester, fluorinating the ester with DAST, brominating the resulting 2,6-difluoro-1-difluoromethoxybenzene, preparing a Grignard reagent from the resulting 4-bromo-2,6-difluoro-1-difluoromethoxybenzene, and reacting the Grignard reagent with t-butyl hydroperoxide or converting the Grignard reagent to a boric ester, and oxidizing the ester with hydrogen peroxide under a basic condition. Alternatively, 3,5-difluoro-4-difluoromethoxyphenol can also be obtained by nitrating 3,5-difluoro-4-difluoromethoxybenzene, reducing the product to 3-fluoro-4-trifluoromethoxyaniline, and decomposing a diazonium salt of the 3-fluoro-4-trifluoromethoxyaniline in sulfuric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05474707
Source datasetuspto-grants-1995_12
ORD IDord-5986e219b93644da9d8bb62e0170853d
Source noteuspto-grants-1995_12