Reaktion #955932

ord-1fc9b3efca8044fdb9cd75ba51fd82b8

Reaktionsgleichung

O=C([O-])O.[Na+]
NaHCO3
Cc1ccc(C(=O)NN)c(C)c1
2,4-dimethylbenzohydrazide
N#CBr
cyanic bromide
Cc1ccc(-c2nnc(N)o2)c(C)c1
5-(2,4-Dimethylphenyl)-1,3,4-oxadiazol-2-amine
Ausbeute 82.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe solution was concentrated
  2. 2
    workup.ADDITIONdiluted with water (20 mL)
  3. 3
    SonstigeThe resulting solid was collected
  4. 4
    Sonstigedried on vacuum

Vorschrift

To a solution of 2,4-dimethylbenzohydrazide (example 16b) (2 g) in dry dioxane (12 mL) was added cyanic bromide (1.28 g, 12.2 mmol) followed by a solution of NaHCO3 (1.02 g, 12.2 mmol) in water (12 mL). The resulting mixture was stirred 2 hours at rt. The solution was concentrated to ½ volume on vacuum and diluted with water (20 mL). The resulting solid was collected and dried on vacuum to give 5-(2,4-Dimethylphenyl)-1,3,4-oxadiazol-2-amine (1.88 g, 82%) as a white solid. 1H NMR (300 MHz, dMSO): δ 2.29 (s, 3H), 2.52 (d, 3H), 7.13 (d, 1H), 7.16 (s, 3H), 7.54-7.56 (d, 1H); MS (M+H, 190).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08968708B2uspto-grants-2015_03