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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1077828Erstellt: 25. Oktober 2026

4-Bromotoluene → 4'-Methyl-biphenyl-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1077828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromotolueneHCID 7805—
EduktDiisobutylaluminum hydrideHCID 14487—
EduktEthyl 3-iodobenzoateHCID 143542—
EduktMagnesiumHCID 5462224—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4'-Methyl-biphenyl-3-carboxylic acid ethyl esterHCID 1072875459,2%

Reaktionsschritte

Magnesium (1.6 g) and p-bromotoluene (10.26 g) in 60 ml of tetrahydrofuran were stirred and warmed until the reaction commenced. When the exothermic reaction had finished, the mixture was refluxed overnight. In a separate flask, 4 ml of DIBAL (1M in toluene) was added to a suspension of bis(triphenylphosphine)palladium(II) chloride (1.4 g) in 100 ml of tetrahydrofuran, followed by ethyl 3-iodobenzoate (11.04 g). To this mixture, the magnesium reagent prepared above was added dropwise, causing an exothermic reaction. The reaction mixture was stirred overnight at room temperature, and then quenched by addition of dilute hydrochloric acid. The mixture was extracted with ether, and the organic layer washed with water, and then saturated brine. The organic layer was separated, dried over sodium sulfate, the solvent evaporated under reduced pressure, and the residue chromatographed on silica gel, eluting with 5% ethyl acetate in heptane, to yield 5.69 g of ethyl 4'-methylbiphenyl-3-carboxylate, a compound of Formula (17), as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05545645
Quelldatensatzuspto-grants-1996_08
ORD IDord-35c48f52b06d4ec986257d5697e09ada
Quellennotizuspto-grants-1996_08