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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1440305Erstellt: 26. Oktober 2026

Ethanol → 1-Bromo-3-isopropoxybenzene

https://huagongshe.com/reaction/1440305

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt2-BromopropaneHCID 6358—
EduktPotassium CarbonateHCID 11430—
Edukt3-BromophenolHCID 11563—
LösungsmittelWaterHCID 962—
Produkt1-Bromo-3-isopropoxybenzeneHCID 326080189,8%

Reaktionsbedingungen

Temperatur78 °C

Reaktionsschritte

The following reagents were combined sequentially: anhydrous ethanol (880 ml), potassium carbonate (448.0 g), 3-bromophenol (386.7 g), 2-bromopropane (400.0 g) and finally water (88 ml). The mixture was heated at reflux (78° C.) for 16 hours. Water (880 ml) was added to the reaction mixture and 900 ml of solvent was removed by distillation at atmospheric pressure during a 4 hour period. Heptane (880 ml) was added to the reaction mixture and later separated. The aqueous layer was extracted with heptane (80 ml) and the combined organic fractions were washed sequentially with 1N HCl (300 ml), water (300 ml), 1N NaOH (300 ml) and water (300 ml). Removal of the solvent by rotary evaporation (50° C., 5 mmHg) afforded 453.6 g (97%) of crude product. This was distilled through a short path distillation column (81°-85° C., 2 mmHg) to provide 431.5 g of the product as a colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05498718
Quelldatensatzuspto-grants-1996_03
ORD IDord-16d25fc307704ba6a20526d0fa153864
Quellennotizuspto-grants-1996_03