Reaktion #618404

ord-3cab66f228bc4199a569c5fd435dacb9

Reaktionsgleichung

O
Water
N#Cc1ccc(Oc2ccc3c(c2)COB3O)cc1
5-(4-cyanophenoxy)-1-hydroxy-2,1-benzoxaborole
[N-]=[N+]=[N-].[Na+]
sodium azide
[Cl-].[NH4+]
ammonium chloride
OB1OCc2cc(Oc3ccc(-c4nnn[nH]4)cc3)ccc21
compound
Ausbeute 23.5%
OB1OCc2cc(Oc3ccc(-c4nnn[nH]4)cc3)ccc21
5-(4-(1H-tetrazol-5-yl)phenoxy)benzo[c][1,2]oxaborol-1(3H)-ol
Ausbeute 23.5%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe mixture was extracted with ethyl acetate
  2. 2
    WaschenThe organic layer was washed with water and brine
  3. 3
    Trocknendried on anhydrous sodium sulfate
  4. 4
    SonstigeThe solvent was removed under reduced pressure
  5. 5
    Sonstigethe residue was purified by silica gel column chromatography (ethyl acetate)

Vorschrift

A mixture of 5-(4-cyanophenoxy)-1-hydroxy-2,1-benzoxaborole (200 mg, 0.797 mmol), sodium azide (103 mg, 1.59 mmol), and ammonium chloride (85 mg, 1.6 mmol) in N,N-dimethylformamide (5 mL) was stirred at 80° C. for two days. Water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried on anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate) followed by trituration with ethyl acetate to give the target compound (55 mg, 23%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09353133B2uspto-grants-2016_05