2-Ethyl-6-methylphenol → 4-Bromo-2-ethyl-6-methylphenol

HRID 323684Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 323684
[CH2:1]([C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:4]=1[OH:10])[CH3:2].[Br-:11].[Br-].[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC>C(Cl)(Cl)Cl>[Br:11][C:7]1[CH:6]=[C:5]([CH3:9])[C:4]([OH:10])=[C:3]([CH2:1][CH3:2])[CH:8]=1

Komponenten

4

Edukt 2

HCID 5193332-Ethyl-6-methylphenolHCID 23500184Tetra-n-butylammonium tribromide

Produkt 1

HCID 220068384-Bromo-2-ethyl-6-methylphenolAusbeute 182,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Then, 16 g of 2-ethyl-6-methylphenol was dissolved in 200 ml of chloroform, which was stirred at 0° C., and 56.6 g of tetrabutylammonium tribromide was added in small portions to this solution. After stirring at room temperature for 1 hour, the solvent was distilled out under reduced pressure. The residue was dissolved in 300 ml of diethyl ether, successively washed with 10% hydrochloric acid and water, dried over anhydrous magnesium sulfate, and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 23 g of 4-bromo-2- ethyl-6-methylphenol (92% yield).

Aufarbeitung

  1. stirringAfter stirring at room temperature for 1 hour
  2. distillationthe solvent was distilled out under reduced pressure
  3. dissolutionThe residue was dissolved in 300 ml of diethyl ether
  4. washsuccessively washed with 10% hydrochloric acid and water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated
  7. customto give a crude product

Quellen und Nachweise

ORD-Eintrag
ord-f0caecc358eb4b89a5c7f398cc8089aa
Quelldatensatz
uspto-grants-2001_04
Patentnummer
US06214835B1

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