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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1620358Erstellt: 26. Oktober 2026

1,3-Dibromopropane → 1,2-Bis(4-(3-bromopropoxy)phenyl)ethane-1,2-dione

https://huagongshe.com/reaction/1620358

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DibromopropaneHCID 8001—
EduktPotassium CarbonateHCID 11430—
Edukt4,4'-DihydroxybenzilHCID 458204—
LösungsmittelDimethylformamideHCID 6228—
Produkt1,2-Bis(4-(3-bromopropoxy)phenyl)ethane-1,2-dioneHCID 68240945—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

1,2-bis(4-hydroxyphenyl)ethane-1,2-dione (2.6 g, 10.74 mmol) was dissolved in DMF and K2CO3 (5.9 g, 42.7 mmol) was added, 100 mmol of 1,3-dibromopropane and a catalytic amount of KI were then added. The mixture was heated to 80° C. and stirred for 3 days. TLC check showed 1,2-bis(4-hydroxyphenyl)ethane-1,2-dione disappeared. Dimethylformamide (DMF) was removed, and water was added, extracted by EtOAc, washed with brine, dried over MgSO4. The solvent was removed and the residue was purified by column chromatography to give 1,2-bis(4-(3-bromopropoxy)phenyl)ethane-1,2-dione 6 as a pale yellow solid, as confirmed by the following nuclear magnetic resonance (NMR) data obtained therefrom: 1H NMR (500 MHz, CDCl3): δ 7.94 (d, J=8.8 MHz, 4H), 6.99 (d, J=8.8 MHz, 4H), 4.20 (t, J=6.2 MHz, 4H), 3.61 (t, J=6.2 MHz, 4H), 2.34 (m, 4H) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08772443B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-a631abe5a25c43389fdf3ed5a2ed2be3
Quellennotizuspto-grants-2014_07