Reaktion #78167

ord-a04317dc604c4abf975d9a0e8fe5f4e4

Reaktionsgleichung

C[O-].[Na+]
sodium methylate
O=C1OCC2=C1CCCC2
4,5,6,7-tetrahydro-1(3H)-isobenzofuranone
O=Cc1ccncc1
pyridine-4-carbaldehyde
CCOC(=O)CC
ethyl propionate
O=C1C2=C(CCCC2)C(=O)C1=C1C=CNC=C1
title compound
O=C1C2=C(CCCC2)C(=O)C1=C1C=CNC=C1
2-[4(1H)-Pyridinylidene]-4,5,6,7-tetrahydro-inden-1,3-dione

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat 0° C
  2. 2
    Temperaturheated for 2 h
  3. 3
    Temperaturunder reflux
  4. 4
    Sonstigeevaporated under vacuum
  5. 5
    workup.STIRRINGStirring of the residue in 5 ml water
  6. 6
    Filtrationfiltration
  7. 7
    Waschenwashing of the filter residue with water
  8. 8
    Sonstigedrying under HV (8 h, 100° C.)

Vorschrift

Four portions each of 0.99 ml 5.4 M methanolic sodium methylate solution (21.4 mmol) are stirred into a solution of 2.957 g (21.4 mmol) 4,5,6,7-tetrahydro-1(3H)-isobenzofuranone (for preparation see J. Am. Chem. Soc. 118, 1-12 [1996]), 2.02 ml (21.4 mmol) pyridine-4-carbaldehyde, and 10.7 ml (93.2 mmol) ethyl propionate in 17.4 ml methanol at intervals of 5 min respectively and at 0° C. The reaction mixture is stirred for 20 min at RT, heated for 2 h under reflux, and then evaporated under vacuum. Stirring of the residue in 5 ml water, filtration, washing of the filter residue with water, and drying under HV (8 h, 100° C.) yields the title compound; m.p. 258-261° C.; ESI-MS: (M+H)+=228. A further, slightly impure batch of title compound may be obtained by extracting the aqueous filtrate with diethylether, adjusting the aqueous phase to pH 7 with glacial acetic acid, filtering, and washing the filter residue with water.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06710047B2uspto-grants-2004_03