Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1668696Erstellt: 26. Oktober 2026

Toluene → 1-Bromo-3-(1-phenylethenyl)benzene

https://huagongshe.com/reaction/1668696

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt3-BromobenzophenoneHCID 70548—
EduktCyclohexane ethylacetateHCID 21867204—
Katalysatormu-Methylene-mu-chlorobis(eta5-2,4-cyclopentadien-1-yl)(dimethylaluminum)titaniumHCID 91617563—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Bromo-3-(1-phenylethenyl)benzeneHCID 23083178—

Reaktionsschritte

To a solution of 3-bromobenzophenone (2.2 g, 8.5 mmol, 1 eq) in 20 mL of dry tetrahydrofuran at 0° C. under N2 atmosphere, was added a toluene solution of the Tebbe's reagent (17 mL of 0.5 M solution, 8.5 mmol, 1 eq.) and the mixture was allowed to warm to room temperature. The reaction mixture was examined after 20 min by TLC (cyclohexane/ethyl acetate 2%) which showed complete conversion to the desired product. Diethyl ether (50 mL) was added and some drops of NaOH 0.1 M aqueous solution was slowly added to quench the reaction. The mixture was dried over magnesium sulfate, passed through a pad of Celite and evaporated. The solid formed was triturated with cyclohexane and filtered; the solution was collected and concentrated under reduced pressure. The crude was purified by flash chromatography eluting with cyclohexane. 2.02 g of clean product was obtained as colorless liquid (yield: 91%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07989449B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-76074725f7b74b019916cb0d779b2f77
Quellennotizuspto-grants-2011_08