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HRID 1885373Erstellt: 26. Oktober 2026

4-Bromotoluene → [1,1'-Biphenyl]-2,5-dicarboxylic acid, 4'-methyl-, 2,5-dimethyl ester

https://huagongshe.com/reaction/1885373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromotolueneHCID 7805—
EduktDimethyl 2-bromoterephthalateHCID 87741—
EduktHCID 178418306HCID 178418306—
KatalysatorZincchlorideHCID 3007855—
KatalysatorHCID 178418751HCID 178418751—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[1,1'-Biphenyl]-2,5-dicarboxylic acid, 4'-methyl-, 2,5-dimethyl esterHCID 10565585,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-Bromotoluene (6 g) was dissolved in tetrahydrofuran (20 ml). To this solution at -78° C. under N2 was added over a ten minute period, 1.7M tBuLi (42 ml). After two hours at room temperature, the reaction mixture was cooled to 0° C. and 1M ZnCl2 (36 ml) was added over a ten minute period. After one half hour at room temperature, bis(triphenylphosphine)nickel(II) chloride (1.32 g) was added followed by dimethyl-2-bromo-terepthalate (6 g) in tetrahydrofuran (20 ml) dropwise over a five minute period. The reaction mixture was stirred at room temperature for two hours. The tetrahydrofuran was removed under reduced pressure. The residue was treated with ethyl acetate and 1N HCl and the layers separated. The organic phase was washed with water, brine, dried over magnesium sulfate and evaporated gave the crude product. Chromatography on silica gel using 5% hexanes/methylene chloride gave the desired product (5.33 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05144028
Quelldatensatzuspto-grants-1992_09
ORD IDord-4bbe740d8d424c48bb5fbfacb76f29ed
Quellennotizuspto-grants-1992_09