Reaktion #10854

ord-040a36dbcef644d3b7a53d23ebd88f75

Reaktionsgleichung

CCOC(=O)CC(=O)OCC
diethyl malonate
[H-].[Na+]
NaH
Cc1ccc(Br)c(F)c1
4-bromo-3-fluorotoluene
Cl
HCl
CCOC(=O)C(C(=O)OCC)c1ccc(C)cc1F
title compound
Ausbeute 59.6%
CCOC(=O)C(C(=O)OCC)c1ccc(C)cc1F
diethyl (2-fluoro-4-methylphenyl)malonate
Ausbeute 59.6%

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITAfter 15 min
  2. 2
    workup.ADDITIONwas added
  3. 3
    TemperaturThe reaction mixture was heated at 100° C. for approximately 15 hours
  4. 4
    Temperaturwas then cooled to 15° C
  5. 5
    Sonstigethe precipitate produced
  6. 6
    Filtrationwas filtered off
  7. 7
    ExtraktionThe filtrate was extracted
  8. 8
    Sonstigethe organic phases, after separation
  9. 9
    Sonstigewere dried

Vorschrift

0.49 mol of diethyl malonate was added at 60° C. inside 2 hours to a mixture of 0.51 mol of NaH and 140 ml of 1,4-dioxane. The mixture was stirred for approximately 10 min at 60° C. and then 0.05 mol of Cu(I)Br was added. After 15 min, a mixture of 0.25 mol of 4-bromo-3-fluorotoluene and 10 ml of 1,4-dioxane was added. The reaction mixture was heated at 100° C. for approximately 15 hours and was then cooled to 15° C. After acidifying with 35 ml of 12N HCl at 15 to 20° C., the precipitate produced was filtered off. The filtrate was extracted and the organic phases, after separation, were dried and then freed from the solvent. 40 g of the title compound were obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07094894B2uspto-grants-2006_08