Reacción #2460306

ord-70ded966e2934b7c8ce1fa495d6fa081

Ecuación de reacción

Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
O=C(O)c1ccc(-c2ccc(C(=O)O)cc2)cc1
biphenyl-4,4′-dicarboxylic acid
CCCCO
n-butanol
Cc1ccccc1
toluene
CCCCOC(=O)c1ccc(-c2ccc(C(=O)OCCCC)cc2)cc1
dibutyl 4,4′-biphenyldicarboxylate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was cooled to ambient,
  2. 2
    Filtraciónfiltered
  3. 3
    Lavadowashed with 10% aqueous NaHCO3
  4. 4
    Secadowith brine, dried (MgSO4)
  5. 5
    Concentraciónconcentrated
  6. 6
    OtroThe crude product was purified by recrystallization from heptane
  7. 7
    Otroto obtain 13.4 g (60% of theory) of colorless crystals

Procedimiento

A mixture of biphenyl-4,4′-dicarboxylic acid (15.2 g, 63 mmol), 100 mL of n-butanol, 200 mL of toluene, and a catalytic amount of p-toluenesulfonic acid was heated at reflux with continuous separation of evolved water (Dean-Stark trap) for 7 d. The reaction mixture was cooled to ambient, diluted with dichloromethane, filtered, washed with 10% aqueous NaHCO3 then with brine, dried (MgSO4), and concentrated. The crude product was purified by recrystallization from heptane to obtain 13.4 g (60% of theory) of colorless crystals. 1H NMR (CDCl3): δ 0.97 (t, 6H), 1.5 (m, 4H), 1.8 (m, 4H), 4.35 (q, 4H), 7.68 (d, 4H), 8.13 (d, 4H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07459263B2uspto-grants-2008_12