Реакция #8694

ord-a49db3e4ff1840bf80f49c0406a40f8c

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added under argon
  2. 2
    ТемператураThe mixture was refluxed for 16 h
  3. 3
    Фильтрацияfiltered
  4. 4
    ДругоеThe filtrate was evaporated
  5. 5
    Другоеthe resulting brown oil was purified on silica gel eluting with heptane:EA 4:1 to 1:1

Методика

(In analogy to a procedure given in J. Am. Chem. Soc. 122 (2000), 1360-1370.) To a suspension of Pd(OAc)2 (455 mg), 2-(di-tert.-butylphosphino)-biphenyl (1.21 g) and K3PO4 (39.6 g) in THF (200 ml) dimethylmalonate (12.85 g) and 1-bromo-3,4-dimethyl-benzene 15.0 g) was added under argon. The mixture was refluxed for 16 h, cooled to rt and diluted with EA (300 ml) and filtered. The filtrate was evaporated and the resulting brown oil was purified on silica gel eluting with heptane:EA 4:1 to 1:1 to give 2-(3,4-dimethyl-phenyl)-malonic acid dimethyl ester (16.2 g) as a colourless oil which slowly crystallises. 1H-NMR (300 MHz, CDCl3): 2.25(s, 3H), 2.26(s, 3H), 3.75(s, 6H), 4.59(s, 1H), 7.10–7.20(m, 3H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091201B2uspto-grants-2006_08