Sulfuric Acid → 5-Hydroxypyridine-2-carbonitrile

HRID 406516

Reaktionsgleichung

Reaktionsgleichung von HRID 406516
S(=O)(=O)(O)O.N[C:7]1[CH:8]=[N:9][C:10]([C:13]#[N:14])=[CH:11][CH:12]=1.N([O-])=[O:16].[Na+]>O.C(OCC)(=O)C>[OH:16][C:7]1[CH:12]=[CH:11][C:10]([C:13]#[N:14])=[N:9][CH:8]=1

Komponenten

6

Edukt 3

HCID 1118Sulfuric AcidHCID 38713955-Aminopyridine-2-carbonitrileHCID 23668193Sodium Nitrite

Produkt 1

HCID 214137735-Hydroxypyridine-2-carbonitrile

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Concentrated sulfuric acid (21.0 mL) was added to a suspension of 3-amino-6-cyanopyridine (5.00 g, 42.0 mmol) in water (75.0 mL), and then a 1.6 M aqueous solution of sodium nitrite (29.0 mL, 46.4 mmol) was slowly added dropwise thereto under ice water cooling. This suspension was stirred for 6 hours at 100° C. The reaction mixture was cooled to room temperature, and then was diluted with ethyl acetate (100 mL). The organic layer was washed sequentially with water and saturated brine, and was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→1:1, v/v). Thus, the title compound was obtained.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to room temperature
  2. washThe organic layer was washed sequentially with water and saturated brine
  3. dry with materialwas dried over anhydrous sodium sulfate
  4. distillationThe solvent was distilled off under reduced pressure
  5. customthe resulting residue was purified by silica gel column chromatography (hexane

Quellen und Nachweise

ORD-Eintrag
ord-1d7052acebb94fe69e24479fd6e409ca
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08754112B2

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