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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 391495Erstellt: 24. Oktober 2026

Benzene → 1,3-Dibenzoylpropane

https://huagongshe.com/de/reaction/391495

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktWaterHCID 962—
EduktPentanedioyl dichlorideHCID 17887—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,3-DibenzoylpropaneHCID 8043227%

Reaktionsschritte

A solution of glutaryl chloride (10 mmol, 1.3 mL) dissolved in anhydrous dichloromethane (20 mL) is introduced into a 100 mL two-necked round-bottomed flask under an inert atmosphere. Aluminum chloride (30 mmol, 4.00 g) is added to the mixture, which immediately turns orange-yellow. A solution of benzene (20 mmol, 1.8 mL) dissolved in anhydrous dichloromethane (10 mL) is added dropwise at room temperature. The solution becomes bright red. The mixture is then refluxed for 24 hours, and turns brown-black. The mixture is then cooled to room temperature and poured into a crystallizing basin containing 20 mL of 10% acidified water, with stirring. A black solid forms, and is filtered off on a Büchner funnel. The yellow organic phase is then extracted with ethyl acetate, dried over MgSO4, filtered, concentrated on a rotary evaporator and recrystallized from 20 mL of methanol. The product obtained is a white solid in a mass of 680 mg. The reaction yield is 27%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383931B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-cd361056b74a4b779691daf7c3b3f2f3
Quellennotizuspto-grants-2013_02