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4-Formylbenzoic acid → 4-((1E)-3-methoxy-3-oxoprop-1-en-1-yl)benzoic acid

HRID 220888
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 220888
[H-].[Na+].[CH:3]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1)=O.C1(P(=[CH:33][C:34]([O:36][CH3:37])=[O:35])(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C1(C)C=CC=CC=1>[CH3:37][O:36][C:34](/[CH:33]=[CH:3]/[C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1)=[O:35]
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Komponenten

5

Edukt 3

HCID 120884-Formylbenzoic acidHCID 17453Acetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 24758Sodium hydride

Produkt 1

HCID 106083304-((1E)-3-methoxy-3-oxoprop-1-en-1-yl)benzoic acidAusbeute 53,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

Sodium hydride (60% dispersion in oil, 1.46 g, 36.6 mmol) was added to a solution of 4-formylbenzoic acid (5.0 g, 33.3 mmol) in toluene (200 ml) and the mixture was stirred for 2 h at room temperature. Methyl (triphenyl-phosphoranylidene)acetate (11.69 g, 35.0 mmol) was added and the mixture was heated at reflux for 20 h. Solvents were removed in vacuo and the residue was redissolved in dichloromethane and 1M NaHCO3. The layers were partitioned and the aqueous layer was acidified with 1M HCl solution then extracted with chloroform. The organic layer was dried and concentrated in vacuo to yield the title compound (3.65 g, 53%).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 20 h
  3. customSolvents were removed in vacuo
  4. dissolutionthe residue was redissolved in dichloromethane
  5. customThe layers were partitioned
  6. extractionthen extracted with chloroform
  7. customThe organic layer was dried
  8. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-f91059fe21ba42e3b176f973ee740d68
Quelldatensatz
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08202858B2

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