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Stannous chloride dihydrate → 3-Amino-2-bromo-5-chloropyridine

HRID 418977
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 418977
[Br:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([Cl:11])=[CH:4][N:3]=1.O.O.[Sn](Cl)Cl>CCOCC.Cl>[Br:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([Cl:11])=[CH:4][N:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 61436Stannous chloride dihydrateHCID 2806812-Bromo-5-chloro-3-nitropyridine

Produkt 1

HCID 27696403-Amino-2-bromo-5-chloropyridineAusbeute 71,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 313Hydrochloric AcidLösungsmittelHCID 3283Diethyl EtherLösungsmittel2×

Versuchsvorschrift

2-Bromo-5-chloro-3-nitro-pyridine (11.87 g, 50 mmol) was dissolved in 100 mL ether. Tin(II) chloride dihydrate (56.4 g, 0.5 mol) was dissolved in 100 mL of concentrated hydrochloric acid and added drop wise over 15 minutes to the stirring ethereal solution of the nitro compound. The exothermic reaction brought the ether to boiling and it was allowed to evaporate off. After the addition was complete the reaction mixture was placed on a 50° C. oil bath and stirred for 30 minutes to boil of the remaining ether. The flask was then cooled on in an ice bath. The precipitate formed was collected and by filtration and dissolved in 100 mL of water. The pH was adjusted to 9-10 by the addition of concentrated ammonium hydroxide solution and the product was extracted with ethyl acetate (2×100 mL). The organic layer was washed with diluted ammonium hydroxide, water and brine and dried over Na2SO4 and the solvent was evaporated to afford 7.4 g of tan crystalline solid. MS m/z: 208.9 (M+H).

Aufarbeitung

  1. customThe exothermic reaction
  2. customto evaporate off
  3. additionAfter the addition
  4. customwas placed on a 50° C.
  5. temperatureThe flask was then cooled on in an ice bath
  6. customThe precipitate formed
  7. filtrationwas collected and by filtration
  8. dissolutiondissolved in 100 mL of water
  9. additionThe pH was adjusted to 9-10 by the addition of concentrated ammonium hydroxide solution
  10. extractionthe product was extracted with ethyl acetate (2×100 mL)
  11. washThe organic layer was washed with diluted ammonium hydroxide, water and brine
  12. dry with materialdried over Na2SO4
  13. customthe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-8e026b7372f2425581d5693218529c39
Quelldatensatz
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08093247B2

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