Benzaldehyde → 5-Hexene-2,4-dione, 6-phenyl-

HRID 1961332

Reaktionsgleichung

Reaktionsgleichung von HRID 1961332
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:9]([CH2:12][C:13](=[O:15])[CH3:14])(=[O:11])[CH3:10].N1CCCCC1>C1CCCCC1>[CH:1](=[CH:14][C:13](=[O:15])[CH2:12][C:9](=[O:11])[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

5

Edukt 3

HCID 240BenzaldehydeHCID 8082PiperidineHCID 31261Acetylacetone

Produkt 1

HCID 27848595-Hexene-2,4-dione, 6-phenyl-

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8078CyclohexaneLösungsmittel

Versuchsvorschrift

Theses compounds may be prepared by various methods but are most conveniently prepared by reacting a benzaldehyde with acetyl acetone in the presence of a suitable catalyst and reaction medium, preferably piperidine and cyclohexane, at reflux temperature under continuous azeotropic water removal. The benzaldehyde reactant will be that which corresponds to the desired substitution of the benzylidene derivative of the final benzylidene pentanedione. The crude product resulting from the foregoing reaction may then be purified by crystallization with methanol to produce the desired benzylidene 2,4-pentanedione. Suitable reactions and reaction conditions are set forth in the examples contained herein.

Aufarbeitung

  1. customTheses compounds may be prepared by various methods
  2. customare most conveniently prepared
  3. temperatureat reflux temperature under continuous azeotropic water
  4. customremoval
  5. customThe crude product resulting from the foregoing reaction
  6. custommay then be purified by crystallization with methanol

Quellen und Nachweise

ORD-Eintrag
ord-269976d36fb9461ebf5535b172927792
Quelldatensatz
uspto-grants-2013_04
Patentnummer
US08414870B2

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