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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430850Erstellt: 24. Oktober 2026

Sulfuric Acid → 3-(2-Bromo-5-methoxy-phenyl)-1-phenyl-propan-1-one

https://huagongshe.com/de/reaction/430850

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktEthyl benzoylacetateHCID 7170—
EduktSodium HydroxideHCID 14798—
EduktSodium ethoxideHCID 2723922—
Edukt2-Bromo-5-methoxybenzyl bromideHCID 3525951—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt3-(2-Bromo-5-methoxy-phenyl)-1-phenyl-propan-1-oneHCID 1139299287%

Reaktionsschritte

To sodium ethoxide (5.72 g, 84 mmol) in 50 ml of anhydrous ethanol was added 14.8 g (77 mmol) of ethyl benzoylacetate with stirring. The reaction mixture was then brought to a gentle reflux and 19.6 g (70 mmol) of 1-Bromo-2-bromomethyl-4-methoxy-benzene in 20 ml of ethanol was added over 20 min. The reaction mixture was refluxed for 2 h. The reaction mixture was cooled, filtered and concentrated. The concentrated mixture was subjected to acid hydrolysis and decarboxylation by refluxing for overnight in a solution containing 40 ml of glacial acetic acid, 5 ml of concentrated sulfuric acid, and 10 ml of water. The reaction mixture was then neutralized with 10% NaOH and extracted with methylene chloride. The extracts were concentrated to give a weight of 19.43 g crude 3-(2-Bromo-5-methoxy-phenyl)-1-phenyl-propan-1-one (yield: 87%). This compound was used in next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06323345B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-381329a12af74001a30c9c130ea804a2
Quellennotizuspto-grants-2001_11