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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399326Generated: October 25, 2026

2,6-Di-tert-butylphenol → 4-Bromo-2,6-di-tert-butylphenol

https://huagongshe.com/reaction/399326

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butylphenolHCID 31405—
ReactantBROMINE CHLORIDE (BrCl)HCID 61697—
Solvent1,2-DichloroethaneHCID 11—
SolventDiethyl EtherHCID 3283—
Product4-Bromo-2,6-di-tert-butylphenolHCID 7082992%

Reaction Steps

To a solution of 2,6-di-tert-butylphenol (2.06 g, 10 mmol) in EDC (50 mL) in a 200-mL round bottom flask, was added the stabilized BrCl brominating reagent (12 mL, about 11 mmol) dropwise, with stirring at room temperature. Initially, the orange reddish color of the reagent disappeared quickly. The color from the last 1 mL persisted for several minutes. The reaction mixture was allowed to stand for 30 minutes before being quenched with a few drops of sodium sulfite solution. After phase separation, it was diluted with EDC (50 mL), washed with water (100 mL) and dried (Na2SO4). The organic layer was concentrated under reduced pressure to afford a glue-like material. The material was redissolved in ether (10 mL) and after solvent removal, a crystalline solid 4-bromo-2,6-di-tert-butylphenol product (2.63 g, 92% recovered yield) was obtained in high purity (>98% by GC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817888
Source datasetuspto-grants-1998_10
ORD IDord-f83b1b5df26c4f0489d308504a235b0f
Source noteuspto-grants-1998_10