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Phosphorus oxychloride → 4-Chloro-5-iodonicotinonitrile

HRID 506173
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 506173
O[C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[CH:4][C:3]=1[I:10].O=P(Cl)(Cl)[Cl:13]>>[Cl:13][C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[CH:4][C:3]=1[I:10]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 178510339HCID 178510339, Verbindung

Produkt 1

HCID 594311594-Chloro-5-iodonicotinonitrileAusbeute 75 %

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of 4-hydroxy-5-iodonicotinonitrile (57.5 g, 234 mmol) and POCl3 (200 mL) was heated at 100° C. for 2 hours, cooled to room temperature and evaporated to remove excess POCl3. The residue was cooled in an ice-water bath, adjusted to pH 8-9 with aqueous 10 N NaOH and extracted with ethyl acetate. The combined organics were washed with water and brine, dried over magnesium sulfate and concentrated. The resulting solid residue was washed with a minimum amount of methanol and methylene chloride to give 46.5 g (75%) of 4-chloro-5-iodonicotinonitrile as a tan solid. Melting range: 120-122° C.

Aufarbeitung

  1. temperaturecooled to room temperature
  2. customevaporated
  3. customto remove excess POCl3
  4. temperatureThe residue was cooled in an ice-water bath
  5. extractionextracted with ethyl acetate
  6. washThe combined organics were washed with water and brine
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated
  9. washThe resulting solid residue was washed with a minimum amount of methanol and methylene chloride

Quellen und Nachweise

ORD-Eintrag
ord-ad1e09b81c2d467d8431361fd21df552
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07781591B2

Notizen zur Reaktion

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