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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorophenol | HCID 6899 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-2,6-dichlorophenol | HCID 18587 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07199265B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-94f8e5998f7c428ab1f681908898c327 |
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| Source note | uspto-grants-2007_04 |
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