4-Phenyl-3-butyn-2-one → HCID 178467506, Verbindung

HRID 1604998Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1604998
[C:1]([C:4]#[C:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:3])[CH3:2].C[Si]([N:16]=[N+:17]=[N-:18])(C)C>CCOCC>[C:1]([C:4]1[N:16]=[N:17][NH:18][C:5]=1[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:3])[CH3:2]

Komponenten

4

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

A mixture of 30 g (0.21 mole) of acetylphenyl-acetylene and 24 g (0.21 mole) of trimethylsilyl azide was heated at 140°C for 24 hours. It was then cooled, dissolved in ether, and extracted with dilute sodium hydroxide. This aqueous layer was separated and made acidic with dilute HCl. The precipitate was recrystallized from benzene-petroleum ether to give 11 g (28%) of 4-acetyl-5-phenyltriazole, m.p. 117°-118°C.

Aufarbeitung

  1. temperatureIt was then cooled
  2. extractionextracted with dilute sodium hydroxide
  3. customThis aqueous layer was separated
  4. customThe precipitate was recrystallized from benzene-petroleum ether

Quellen und Nachweise

ORD-Eintrag
ord-208daa7bc6674a70a9370a464c2a0e47
Quelldatensatz
uspto-grants-1976_04
Patentnummer
US03948929

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