تفاعل #454250

ord-d48e04a6b9e3451dbb0d88112d5e86f9

معادلة التفاعل

Oc1cncc(Br)c1
5-Bromo-3-pyridinol
[K+].[OH-]
KOH
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
O=[N+]([O-])c1ccc(N=Nc2ncc(O)cc2Br)cc1
3-Bromo-2-(4-nitrophenylazo)-5-hydroxypyridine

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    ترشيحfiltered
  3. 3
    أخرىto air dry
  4. 4
    أخرىchromatographed (silica gel; chloroform/methanol, 95:5-90:10)

الإجراء التجريبي

5-Bromo-3-pyridinol from Example 12b (8.7 g, 0.050 mmol) and KOH (1.1 g, 19.6 mmol) were dissolved in water (200 mL). A suspension of p-nitrobenzenediazonium tetrafluoroborate (11.8 g, 0.50 mol, prepared as described in J. Org. Chem., 44: 1572-15783 (1979)) was added. The reaction was stirred for 1 hour, diluted with acetic acid (50 mL) and filtered. The crude product was allowed to air dry, then chromatographed (silica gel; chloroform/methanol, 95:5-90:10) to provide the title compound (5.45 g, 34% yield): MS (CI/NH3) m/z 323, 325 (M+H)+ ; NMR (DMSO-d6, 300 MHz) δ 8.48-8.43 (m, 2H), 8.21 (d, J=2.4 Hz, 1H), 8.09-8.06 (m, 2H), 7.72 (d, J=2.4 Hz, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06133253uspto-grants-2000_10