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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028987Generated: October 30, 2026

Hydrogen Bromide → HCID 44891120, compound

https://huagongshe.com/reaction/1028987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantEthanolHCID 702—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 86676840HCID 86676840—
Catalystcopper(I) bromideHCID 24593—
ProductHCID 44891120HCID 44891120—

Reaction Steps

A solution of 2-bromo-4-fluoro-6-methylaniline HCl (5.0 g, 17.6 mmol) in 25% aq. HBr (38.1 mL, 175 mmol) was cooled to 0° C. and an aq. solution of sodium nitrite (0.59 mL, 18.4 mmol) added, followed by a small amount of EtOH to aid solubility. The reaction was stirred at this temperature for 25 min before transferring by pipette to a solution of copper(I) bromide (2.64 g, 18.4 mmol) in 25% aq. HBr (20 ml) at 70° C. The reaction was stirred at this temperature for 3 h. The reaction was quenched with NaHCO3 and the aqueous layer was extracted with EtOAc. The organic layer was then washed with water and brine (3× ea.), dried over Na2SO4 and concentrated in vacuo. The crude material was purified by column chromatography (0-10% Hexene/EtOAC) to yield 1,2-dibromo-5-fluoro-3-methylbenzene as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-0be93410a5214c76a3a172bac8ea4e1a
Source noteuspto-grants-2014_05