Hydrogen Bromide → 2-Bromo-1-phenyl-2-pyrid-4-ylethanone

HRID 80734Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 80734
[C:1]1([C:7](=[O:15])[CH2:8][C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BrH:16].BrBr>C(O)(=O)C>[Br:16][CH:8]([C:9]1[CH:10]=[CH:11][N:12]=[CH:13][CH:14]=1)[C:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:15]

Komponenten

5

Edukt 3

HCID 260Hydrogen BromideHCID 24408BromineHCID 2871041-Phenyl-2-(4-pyridinyl)ethanone

Produkt 1

HCID 134660102-Bromo-1-phenyl-2-pyrid-4-ylethanone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel3×

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of 36 g (182 mmol) of 1-phenyl-2-pyrid-4-ylethanone in 350 mL of acetic acid are successively added at room temperature 28 ml (210 mmol) of a solution containing 30% by weight of hydrobromic acid in acetic acid and 10.1 ml (197 mmol) of bromine dissolved in 50 mL of acetic acid. The solution is heated at 60° C. for one hour and then cooled. The product is precipitated by adding diethyl ether, and 63 g of a yellow solid are isolated after drying.

Aufarbeitung

  1. temperaturecooled
  2. customThe product is precipitated
  3. additionby adding diethyl ether, and 63 g of a yellow solid
  4. customare isolated
  5. customafter drying

Quellen und Nachweise

ORD-Eintrag
ord-4430004097404aef878782f7392ab0a5
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846676B2

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