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Oxalyl chloride → Methyl 2,6-dichloro-5-fluoronicotinate

HRID 610241
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 610241
[Cl:1][C:2]1[N:10]=[C:9]([Cl:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[C:13](Cl)(=O)C(Cl)=O>CN(C)C=O.ClCCl>[Cl:1][C:2]1[N:10]=[C:9]([Cl:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4]([O:6][CH3:13])=[O:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 65578Oxalyl chlorideHCID 27336592,6-Dichloro-5-fluoronicotinic acid

Produkt 1

HCID 2775354Methyl 2,6-dichloro-5-fluoronicotinate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideKatalysatorHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To 60 ml of dichloromethane were added 21.0 g of 2,6-dichloro-5-fluoronicotinic acid, 10 ml of oxalylchloride, and 10 drops of N,N-dimethylformamide, and the mixture was stirred at room temperature for one day. The solvent and the excess reagents were distilled off under reduced pressure, and the residue was dissolved in 50 ml of chloroform. 10 ml of methanol was added dropwise to the solution, and the solution was stirred at room temperature for 60 minutes, and 15 g of anhydrous potassium carbonate was added to the solution and the solution was stirred for another 30 minutes. The solution was separated by adding 150 ml of chloroform and 150 ml of distilled water, and the chloroform layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain 26.6 g of the title compound as a colorless crude oily residue.

Aufarbeitung

  1. distillationThe solvent and the excess reagents were distilled off under reduced pressure
  2. dissolutionthe residue was dissolved in 50 ml of chloroform
  3. addition10 ml of methanol was added dropwise to the solution
  4. stirringthe solution was stirred at room temperature for 60 minutes
  5. addition15 g of anhydrous potassium carbonate was added to the solution
  6. stirringthe solution was stirred for another 30 minutes
  7. customThe solution was separated
  8. additionby adding 150 ml of chloroform and 150 ml of distilled water
  9. dry with materialthe chloroform layer was dried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-56063af7fe5042f199869ae48d4fdf45
Quelldatensatz
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05998436

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