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Ethanol → N-(6-chloro-2-methoxypyridin-3-yl)formamide

HRID 546742
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 546742
[Cl-].[NH4+].[Cl:3][C:4]1[N:9]=[C:8]([O:10][CH3:11])[C:7]([N+:12]([O-])=O)=[CH:6][CH:5]=1.[CH2:15]([OH:17])C>O.[Fe]>[Cl:3][C:4]1[N:9]=[C:8]([O:10][CH3:11])[C:7]([NH:12][CH:15]=[O:17])=[CH:6][CH:5]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 107977036-Chloro-2-methoxy-3-nitropyridine

Produkt 1

HCID 86628511N-(6-chloro-2-methoxypyridin-3-yl)formamide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23925IronKatalysatorHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

Iron (11.9 g) and ammonium chloride (22.7 g) were added to a solution of 6-chloro-2-methoxy-3-nitropyridine (10.0 g, CAS: 40851-91-0) in ethanol (130 mL) and water (52 mL). The reaction solution was stirred at 80 to 90° C. for one hour and 20 minutes and then left to cool to room temperature. The reaction solution was filtered through celite and washed with ethanol. Then, the filtrate was concentrated under reduced pressure. The residue was diluted with ethyl acetate and water, and the organic layer was separated. The resulting organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was diluted with THF (26 mL). The THF solution was added dropwise to a mixed solution of formic acid (20.1 mL) and acetic anhydride (20.1 mL) at room temperature. Then, the reaction solution was stirred for one hour. Ice water (120 mL) was added to the reaction solution, and the precipitated crystals were collected by filtration. The crystals were washed with water and then air-dried to obtain 5.85 g of the title compound. The property value of the compound is as follows.

Aufarbeitung

  1. waitleft
  2. temperatureto cool to room temperature
  3. filtrationThe reaction solution was filtered through celite
  4. washwashed with ethanol
  5. concentrationThen, the filtrate was concentrated under reduced pressure
  6. additionThe residue was diluted with ethyl acetate and water
  7. customthe organic layer was separated
  8. washThe resulting organic layer was washed with brine
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. additionThe residue was diluted with THF (26 mL)
  12. additionThe THF solution was added dropwise to a mixed solution of formic acid (20.1 mL) and acetic anhydride (20.1 mL) at room temperature
  13. stirringThen, the reaction solution was stirred for one hour
  14. additionIce water (120 mL) was added to the reaction solution
  15. filtrationthe precipitated crystals were collected by filtration
  16. washThe crystals were washed with water
  17. customair-dried

Quellen und Nachweise

ORD-Eintrag
ord-95c81ef0cc344068a6384be254aee93b
Quelldatensatz
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07935815B2

Notizen zur Reaktion

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