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

Temperatur

0 °C

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-terephthalate (6 g) in tetrahydrofuran 920 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 which gave the crude product. Chromatography on silica gel using 5% hexanes/methylene chloride gave the desired product (5.33 g).

1. additionTo this solution at -78° C. under N2 was added over a ten minute period
2. waitAfter one-half hour at room temperature
3. customdropwise over a five minute
4. customThe tetrahydrofuran was removed under reduced pressure
5. additionThe residue was treated with ethyl acetate and 1N HCl
6. customthe layers separated
7. washThe organic phase was washed with water, brine
8. dry with materialdried over magnesium sulfate
9. customevaporated which
10. customgave the crude product

ORD-Eintrag

ord-be81bf75d1fc4acba37136f7bcfb08e4

Quelldatensatz

uspto-grants-1994_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05356889