Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342977Generated: October 30, 2026

Hydrogen Bromide → 1-Bromo-2-chloro-4-(trifluoromethoxy)benzene

https://huagongshe.com/reaction/342977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2-Chloro-4-(trifluoromethoxy)anilineHCID 2734084—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product1-Bromo-2-chloro-4-(trifluoromethoxy)benzeneHCID 53414034—

Reaction Steps

A solution of sodium nitrite (16.31 g) in concentrated sulphuric acid was added dropwise to a solution of 2-chloro-4-trifluoromethoxyaniline (50 g) in acetic acid, while maintaining the temperature below 10° C. The mixture was stirred at 5°-10° C. for 0.5 hours then added slowly to a mixture of cuprous bromide (33.9 g) in aqueous hydrobromic acid (200 ml) and ice. The mixture was stirred at room temperature for 0.5 hours and left to stand overnight. The mixture was diluted with water and extracted with dichloromethane, washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 2-chloro-4-trifluoromethoxybromobenzene (63.64 g) as a brown oil which was not further purified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859283
Source datasetuspto-grants-1999_01
ORD IDord-be70d093f5cd4d11af9348bb3408e6fd
Source noteuspto-grants-1999_01