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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259533Generated: October 30, 2026

Hydrogen Peroxide → 4-Chloro-3,5-difluoroaniline

https://huagongshe.com/reaction/2259533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactanttert-Butyl hydroperoxideHCID 6410—
Reactant2,6-DifluoroanilineHCID 79647—
ReactantBenzene, 2-chloro-1,3-difluoro-HCID 142257—
Reactant5-Bromo-2-chloro-1,3-difluorobenzeneHCID 2773258—
Reactant4-Chloro-3,5-difluorophenolHCID 19436620—
SolventHydrochloric AcidHCID 313—
Product4-Chloro-3,5-difluoroanilineHCID 19436621—

Reaction Steps

Compound (250) can be prepared in the same manner as in Preparation Example 240, except for replacing compound (P102) with 4-chloro-3,5-difluorophenol. The 4-chloro-3,5-difluorophenol can be prepared by reacting a Grignard reagent prepared from 1-bromo-4-chloro-3,5-difluorobenzene with t-butyl hydroperoxide or converting the same Grignard reagent to a boric ester, and oxidizing the product with hydrogen peroxide under a basic condition. It is also prepared by nitrating 2-chloro-1,3-difluorobenzene (obtainable by decomposing a diazonium salt of 2,6-difluoroaniline in the presence of cuprous chloride or in hydrochloric acid), reducing the nitro-compound to obtain 4-chloro-3,5-difluoroaniline, and decomposing its diazonium salt in sulfuric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05474707
Source datasetuspto-grants-1995_12
ORD IDord-1d1a709b043a4d45a68f0961ea7e2b42
Source noteuspto-grants-1995_12