تفاعل #453041

ord-170b365ee639478d9fde5020246fa61f

معادلة التفاعل

Oc1cncc(Br)c1
5-bromo-3-pyridinol
[K+].[OH-]
potassium hydroxide
F[B-](F)(F)F.N#[N+]c1ccc([N+](=O)[O-])cc1
p-nitrobenzenediazonium tetrafluoroborate
O=[N+]([O-])c1ccc(N=Nc2ncc(O)cc2Br)cc1
title compound
المردود 33.7%
O=[N+]([O-])c1ccc(N=Nc2ncc(O)cc2Br)cc1
5-Hydroxy-3-bromo-2-(4-nitrophenylazo)pyridine
المردود 33.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITION1979 p 1572-1573) (11.845 g, 0.5 mol) was added
  2. 2
    ترشيحfiltered
  3. 3
    أخرىto dry in air
  4. 4
    أخرىwas chromatographed (silica gel; CHCl3/MeOH, 95:5 to 90:10)

الإجراء التجريبي

5-bromo-3-pyridinol (8.7 g, 0.05 mol) and potassium hydroxide (Fisher Scientific) were dissolved in water (200 ml). A suspension of p-nitrobenzenediazonium tetrafluoroborate (J. Org. Chem., Vol. 44, No 9. 1979 p 1572-1573) (11.845 g, 0.5 mol) was added, and the mixture was stirred for 1 hour, diluted with acetic acid (50 ml) and filtered. The crude product was allowed to dry in air, then was chromatographed (silica gel; CHCl3/MeOH, 95:5 to 90:10) provided 5.45g (33.7 %) of the title compound. MS (CI/NH3) m/e 323/325 (M+H)+. 1H NMR (DMSO-d6, 300 MHz) δ8.48-8.43 (m, 2H), 8.21-8.20 (d, J=2.37 Hz, 1H) 8.09-8.06 (m, 2H), 7.72-7.71 (d, J=2.37 Hz, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06127386uspto-grants-2000_10