Diphenylacetylene → HCID 178420171, Verbindung

HRID 1287653

Reaktionsgleichung

Reaktionsgleichung von HRID 1287653
[C:1]1([C:7]#[C:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C[Si]([N:19]=[N+:20]=[N-:21])(C)C>>[C:1]1([C:7]2[N:19]=[N:20][NH:21][C:8]=2[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Komponenten

3

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

A mixture of 50 g (0.28 moles) of diphenylacetylene and 33 g (0.28 moles) of trimethylsilylazide was heated at 150°C for several days. The cooled reaction mixture was extracted with hot dilute NaOH. This was washed with toluene while still warm, cooled, and acidified. The precipitate was recrystallized from toluene to give 17 g of 4,5-diphenyl-1,2,3(1H)-triazole, m.p. 131°C.

Aufarbeitung

  1. customThe cooled reaction mixture
  2. extractionwas extracted with hot dilute NaOH
  3. washThis was washed with toluene
  4. temperaturewhile still warm
  5. temperaturecooled
  6. customThe precipitate was recrystallized from toluene

Quellen und Nachweise

ORD-Eintrag
ord-eecb2c9d46de49d48d1ccae59357b559
Quelldatensatz
uspto-grants-1976_10
Patentnummer
US03985765

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