3-Methyl-2,4-pentanedione → HCID 178424484, Verbindung

HRID 1813923Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1813923
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[C:3]=1[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH2:16].C[CH:18]([C:22](=O)[CH3:23])[C:19](=[O:21])C>>[CH3:23][C:22]1[CH:18]=[C:19]([OH:21])[C:12]2[C:11](=[C:10]([C:3]3[C:4]([CH3:9])=[CH:5][C:6]([CH3:8])=[CH:7][C:2]=3[CH3:1])[CH:15]=[CH:14][CH:13]=2)[N:16]=1

Komponenten

3

Edukt 2

HCID 699493-Methyl-2,4-pentanedioneHCID 137578442-(2,4,6-Trimethylphenyl)aniline

Produkt 1

HCID 178424484HCID 178424484, Verbindung

Reaktionsbedingungen

Temperatur
170 °C

Versuchsvorschrift

A mixture of 2′,4′,6′-trimethyl-biphenyl-2-ylamine(607 mg, 2.88 mmol) and methyl acetylacetone (607 mg, 5.75 mmol) in polyphosphoric acid (3 ml) was heated in 170° C. oil bath for 2.5 hours. The mixture was quenched with water and extracted twice with chloroform. The organic layer was washed with brine, dried and concentrated to give the title compound as an oil. The oil was pumped in vacuo, then trituated with a mixture of ether and hexane to give 642 mg (81%) of the title compound as a beige solid. The solid was recrystallized from ethyl acetate to give a beige solid, mp>250° C.

Aufarbeitung

  1. customThe mixture was quenched with water
  2. extractionextracted twice with chloroform
  3. washThe organic layer was washed with brine
  4. customdried
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-f5babae7267c4e94846f1761de8ceb10
Quelldatensatz
uspto-grants-2005_04
Patentnummer
US06875769B2

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