Pyridine N-Oxide → Methyl 3,3-dimethyl-5-oxovalerate

HRID 1290298

Reaktionsgleichung

Reaktionsgleichung von HRID 1290298
Br[CH2:2][CH2:3][C:4]([CH3:11])([CH3:10])[CH2:5][C:6]([O:8][CH3:9])=[O:7].[N+]1([O-:18])C=CC=CC=1.C(=O)(O)[O-].[Na+].C(=O)([O-])[O-].[NH4+].[NH4+]>C1(C)C=CC=CC=1.O>[CH3:10][C:4]([CH3:11])([CH2:3][CH:2]=[O:18])[CH2:5][C:6]([O:8][CH3:9])=[O:7]

Komponenten

7

Versuchsvorschrift

A mixture of methyl 5-bromo-3,3-dimethylpentanoate (5.0 g), pyridine-N-oxide (4.49 g), sodium bicarbonate (3.77 g) and toluene (30 cm3) was heated at the reflux temperature with vigorous agitation for a period of 14 hours. After cooling the mixture to the ambient temperature, water (20 cm3), saturated ammonium carbonate solution (20 cm3) and toluene (50 cm3) were added and the aqueous phase separated and extracted with toluene (3×75 cm3). The toluene extracts were added to the main organic phase and the whole dried over anhydrous magnesium sulphate concentrated by evaporation of the more volatile components under reduced pressure. The residual liquid was purified by Kugelrohr distillation (130° C./water pump pressure) to give methyl 3,3-dimethyl-5-oxopentanoate in 63% yield.

Aufarbeitung

  1. temperaturewas heated at the reflux temperature with vigorous agitation for a period of 14 hours
  2. additionwere added
  3. customthe aqueous phase separated
  4. extractionextracted with toluene (3×75 cm3)
  5. additionThe toluene extracts were added to the main organic phase
  6. dry with materialthe whole dried over anhydrous magnesium sulphate
  7. concentrationconcentrated by evaporation of the more volatile components under reduced pressure
  8. distillationThe residual liquid was purified by Kugelrohr distillation (130° C./water pump pressure)

Quellen und Nachweise

ORD-Eintrag
ord-9f168e7594f146d59b75304cfdc50861
Quelldatensatz
uspto-grants-1998_05
Patentnummer
US05750769

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