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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1457598Erstellt: 25. Oktober 2026

Ethyl Bromide → 2-tert-Butyl-4-ethoxyphenol

https://huagongshe.com/reaction/1457598

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktTert-ButylhydroquinoneHCID 16043—
EduktSodium hydrideHCID 24758—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-tert-Butyl-4-ethoxyphenolHCID 1242364822%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A mixture of 19.85 g of tert-butylhydroquinone, 10.7 ml of ethyl bromide and 200 ml of dimethylformamide (DMF) was cooled to -78° C., and 4.82 g of 62.5% sodium hydride was added to the mixture. The temperature of the mixture was raised to 0° C., and the mixture was further stirred under ice-cooling for 30 minutes. The reaction mixture was poured into ice water, and the mixture was extracted with ethyl acetate. The extract was washed and dried, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (solvent; hexane:ethyl acetate=10:1), and recrystallized from hexane to give 5.045 g of 4-ethoxy-2-tert-butylphenol (yield: 22%, melting point: 96°-98° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05849732
Quelldatensatzuspto-grants-1998_12
ORD IDord-0fcf3e76e20648fda250e06bb1d928a5
Quellennotizuspto-grants-1998_12