Acetic Acid → 5-(4-Bromophenyl)-1H-1,2,4-triazole

HRID 538988

Reaktionsgleichung

Reaktionsgleichung von HRID 538988
O.[NH2:2]N.C(O)(=O)C.[Br:8][C:9]1[CH:21]=[CH:20][C:12]([C:13](/[N:15]=[CH:16]/[N:17](C)C)=O)=[CH:11][CH:10]=1>>[Br:8][C:9]1[CH:21]=[CH:20][C:12]([C:13]2[NH:2][N:17]=[CH:16][N:15]=2)=[CH:11][CH:10]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a solution of hydrazine hydrate (1.96 mL, 40.4 mmol) in acetic acid (91.9 mL, 36.8 mmol) was added (E)-4-bromo-N-((dimethylamino)methylene)benzamide (9.38 g, 36.8 mmol) and the mixture stirred at 90° C. for 1.5 hours. The reaction mixture was concentrated to about 10 mL and diluted with ether (50 mL). The resulting white solid was collected by vacuum filtration, rinsing with excess ether, and dried to afford 5-(4-bromophenyl)-1H-1,2,4-triazole (5.48 g, 66%) which was carried on without further purification. LCMS (APCI+) m/z 224, 226 [M+H]+.

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated to about 10 mL
  2. additiondiluted with ether (50 mL)
  3. filtrationThe resulting white solid was collected by vacuum filtration
  4. washrinsing with excess ether
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-a03b0807d0e747069a523bbc344bccc7
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08865726B2

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