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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42396Erstellt: 24. Oktober 2026

1,4-Dibromobutane → 2-(3-(4-Bromobutyl)phenyl)-1,3-dioxolane

https://huagongshe.com/de/reaction/42396

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DibromobutaneHCID 8056—
Edukt2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
EduktHCID 178418306HCID 178418306—
Produkt2-(3-(4-Bromobutyl)phenyl)-1,3-dioxolaneHCID 58028468—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

To a clean and dry 2000 ml round bottom flask equipped with a 500 ml addition funnel, low temperature thermometer and magnetic stir bar was transferred anhydrous tetrahydrofuran (800.0 ml) under nitrogen. 2-(3-bromophenyl)-1,3-dioxolane (33.0 ml, 0.2183 mol) was added to this flask by syringe. The reaction vessel was placed into a dry ice/acetone bath until a temperature of <−65° was achieved. The reaction mixture was then allowed to stir for 45 minutes at a stirring speed of 550 rpm in order to verify the integrity of the stirring apparatus at this temperature. Tert-butyllithium solution (257.0 ml, 0.4690 mol) was transferred to the addition funnel by cannula, then added drop wise to the reaction never allowing the temperature to rise above −65° C. Following addition, the reaction was allowed to stir for a period of 30 minutes. The vessel was then removed from the dry ice/acetone bath and allowed to warm to a temperature of −20° C. The vessel was then again placed into the dry ice/acetone bath until a temperature of <−65° was achieved. 1,4-dibromobutane (103.5 ml, 0.8740 mol) was added to the reaction dropwise via syringe, maintaining the current temperature. The reaction was allowed to stir for 30 minutes at this temperature following addition. The reaction was slowly warmed to room temperature over the following 12 hours. After warming, the reaction was quenched by the addition of isopropanol (20.0 ml) via syringe.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08535974B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-04769ea0cd3040258ed0ef6b88653b08
Quellennotizuspto-grants-2013_09