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Methanol → Methyl 3-bromoisonicotinate Hydrochloride

HRID 31393
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 31393
Cl.[Br:2][C:3]1[CH:11]=[N:10][CH:9]=[CH:8][C:4]=1[C:5]([OH:7])=[O:6].S(Cl)([Cl:14])=O.[CH3:16]O>C(OCC)(=O)C.CN(C=O)C>[ClH:14].[Br:2][C:3]1[CH:11]=[N:10][CH:9]=[CH:8][C:4]=1[C:5]([O:7][CH3:16])=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 684306873-Bromoisonicotinic Acid Hydrochloride

Produkt 1

HCID 68433567Methyl 3-bromoisonicotinate Hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideKatalysatorHCID 8857Ethyl Acetate
Lösungsmittel

Versuchsvorschrift

To a stirred suspension of 3-bromoisonicotinic acid hydrochloride (27.4 g, 0.10 mol) in ethyl acetate (250 ml) was added one drop of DMF followed by thionyl chloride (18.5 g, 0.16 mol). The mixture was heated at reflux for 1 h and allowed to cool to room temperature. The mixture was then concentrated under reduced pressure to give an off-white solid. To this was added methanol and this was refluxed for 2 hrs. The mixture was then concentrated under reduced pressure and diluted with ethyl acetate. The precipitate was collected on filter paper on a Buchner funnel. The white solid was washed with ethyl acetate and air-dried. The white solid was placed in a vacuum oven at 60° C. overnight with a nitrogen bleed. Yield: 18.5 g (71% th).

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 1 h
  3. concentrationThe mixture was then concentrated under reduced pressure
  4. customto give an off-white solid
  5. temperaturethis was refluxed for 2 hrs
  6. concentrationThe mixture was then concentrated under reduced pressure
  7. additiondiluted with ethyl acetate
  8. customThe precipitate was collected
  9. filtrationon filter paper on a Buchner funnel
  10. washThe white solid was washed with ethyl acetate
  11. customair-dried

Quellen und Nachweise

ORD-Eintrag
ord-12017e20021f467a8b28a740c514cdfb
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07425639B2

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