Reaktion #1435727

ord-e37e69539bc748cbb6d02b9052e3096e

Reaktionsgleichung

Cl
hydrochloric acid
[H-].[Na+]
sodium hydride
CCOC(=O)OCC
diethyl carbonate
CCOC(=O)Cc1c(F)cccc1Cl
ethyl 2-chloro-6-fluorophenylacetate
CCOC(=O)C(C(=O)OCC)c1c(F)cccc1Cl
diethyl (2-chloro-6-fluorophenyl)malonate
Ausbeute 87.7%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwere added dropwise
  2. 2
    Temperaturunder heating
  3. 3
    Temperaturrefluxed
  4. 4
    Temperaturunder heating for 8 hours
  5. 5
    TemperaturThe reaction mixture was cooled
  6. 6
    Extraktionextracted with t-butyl methyl ether
  7. 7
    WaschenThe organic layer was washed with water
  8. 8
    Trocknendried over sodium sulfate
  9. 9
    Einengenconcentrated

Vorschrift

Into a mixture of 7.2 g of sodium hydride (60% in oil), 17.0 g of diethyl carbonate and 150 ml of tetrahydrofuran, 26.0 g of ethyl 2-chloro-6-fluorophenylacetate were added dropwise under heating, and then refluxed under heating for 8 hours. The reaction mixture was cooled, poured into iced dil. hydrochloric acid and extracted with t-butyl methyl ether. The organic layer was washed with water, dried over sodium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 30.4 g of diethyl (2-chloro-6-fluorophenyl)malonate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07211545B2uspto-grants-2007_05