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Thionyl bromide → 4-(Bromomethyl)-3,5-difluoropyridine

HRID 578883
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 578883
[F:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([F:10])[C:7]=1[CH2:8]O.S(Br)([Br:13])=O>C(Cl)Cl.CN(C=O)C>[Br:13][CH2:8][C:7]1[C:2]([F:1])=[CH:3][N:4]=[CH:5][C:6]=1[F:10]
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Komponenten

5

Edukt 2

HCID 68176Thionyl bromideHCID 66815317(3,5-Difluoropyridin-4-yl)methanol

Produkt 1

HCID 668150974-(Bromomethyl)-3,5-difluoropyridine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideKatalysatorHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

(3,5-Difluoro-4-pyridyl)methanol (6.11 g, 42.11 mmol) was dissolved in CH2Cl2 (140 mL). At 0° C. Thionyl bromide (3.589 mL, 46.32 mmol) was added slowly, then 1 drop of DMF was added: the solution turned yellow with gas evolution. The reaction mixture was stirred at rt for 1.5 h. It was quenched with 10 ml water. The pH was made basic (pH=9) with aq NaHCO3. The water layer was extracted 3 times with CH2Cl2. The combined organic layers were washed with brine. The organic phase was dried with Na2SO4, filtrated and the filtrate evaporated. The desired product was obtained as a brown liquid (9.68 g, lacrimator).

Aufarbeitung

  1. customAt 0° C
  2. customIt was quenched with 10 ml water
  3. extractionThe water layer was extracted 3 times with CH2Cl2
  4. washThe combined organic layers were washed with brine
  5. dry with materialThe organic phase was dried with Na2SO4
  6. filtrationfiltrated
  7. customthe filtrate evaporated

Quellen und Nachweise

ORD-Eintrag
ord-ea3b8cd878e34e4f8bdae6b7f8cf2e5c
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09040708B2

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