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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269554Generated: October 29, 2026

2,6-Dichlorophenol → 4-Bromo-2,6-dichlorophenol

https://huagongshe.com/reaction/1269554

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorophenolHCID 6899—
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
SolventAcetonitrileHCID 6342—
Product4-Bromo-2,6-dichlorophenolHCID 18587—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mechanically stirred solution of 2,6-dichlorophenol (100 g) in acetonitrile (400 mL) was cooled to 0° C. and bromine (108 g) in acetonitrile (100 mL) was added dropwise. The red solution was stirred at 0° C. for an additional two hours and an saturated aqueous solution of sodium sulphite was added until the red color disappeared. The phases were separated and the aqueous phase was extracted three times with ethyl acetate. Concentration of the combined organic phases gave 4-bromo-2,6-dichlorophenol as a yellow oil, which crystallized on standing. The crystalline material was washed with water and dried to give 126 g (85%) of colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199265B2
Source datasetuspto-grants-2007_04
ORD IDord-94f8e5998f7c428ab1f681908898c327
Source noteuspto-grants-2007_04