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HRID 399326Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/399326

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-Di-tert-butylphenolHCID 31405—
EduktBROMINE CHLORIDE (BrCl)HCID 61697—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelDiethyl EtherHCID 3283—
Produkt4-Bromo-2,6-di-tert-butylphenolHCID 7082992%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05817888
Quelldatensatzuspto-grants-1998_10
ORD IDord-f83b1b5df26c4f0489d308504a235b0f
Quellennotizuspto-grants-1998_10