Reaktion #2328973

ord-f4cd204983fb49668dac22bb9a715352

Reaktionsgleichung

COC=C1CCC(C(=O)OC)CC1
methyl 4-methoxymethylidenecyclohexanecarboxylate
Cl
hydrochloric acid
CCCCCC
hexane
COC(=O)C1CCC(C=O)CC1
methyl 4-formylcyclohexanecarboxylate
Ausbeute 97.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe aqueous layer was extracted with ethyl acetate
  2. 2
    Waschenby washing in turn with water and saturated saline
  3. 3
    TrocknenThe mixture was dried over anhydrous sodium sulfate
  4. 4
    Einengenconcentrated

Vorschrift

103 g of methyl 4-methoxymethylidenecyclohexanecarboxylate was dissolved in 350 mL of THF and 100 mL of 10% hydrochloric acid was added dropwise at 11 to 13° C. over 10 minutes. After stirring at room temperature for 3 hours, 80 mL of hexane was added. The aqueous layer was extracted with ethyl acetate and then combined with the organic layer, followed by washing in turn with water and saturated saline. The mixture was dried over anhydrous sodium sulfate and concentrated to obtain 92.4 g of methyl 4-formylcyclohexanecarboxylate as an oily substance. The gas chromatography analysis revealed that the resulting substance is a mixture of a cis isomer and a trans isomer in a mixing ratio of 64:36.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07670504B2uspto-grants-2010_03