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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670809Generated: October 25, 2026

Hydrogen Bromide → 5-Bromo-1,3-dichloro-2-methylbenzene

https://huagongshe.com/reaction/1670809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant3,5-Dichloro-4-methylanilineHCID 641154—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-1,3-dichloro-2-methylbenzeneHCID 64115545%

Reaction Steps

Suspend 3,5-dichloro-4-methylaniline in 48% HBr (5 mL) and water (5 mL) and heat with a heat gun until the mixture is near the boiling point. Cool the slurry to room temperature and then cool to 0° C. with an ice/brine bath. Add dropwise a solution of sodium nitrite (109 mg, 1.58 mmol) in water (2 mL). After the addition is complete, stir the reaction an additional 15 min in the cold bath. Add a solution of CuBr (1.08 g, 7.53 mmol) in 48% HBr (2 mL) and heat the rapidly stirring reaction to 50° C. for 1 hour. Cool the reaction to room temperature, dilute with EtOAc and discard the aqueous layer. Wash the organic layer with water and brine, dry with MgSO4, filter through celite and concentrate to an orange residue. Purify the residue by silica gel chromatography eluting with hexanes to afford 164 mg (45%) of the product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994176B2
Source datasetuspto-grants-2011_08
ORD IDord-c159d6a41741433ebf97aa3d280c2207
Source noteuspto-grants-2011_08