1,2-Dichloroethane → 1-(4-Bromo-2-fluorophenyl)-3-chloro-1-propanone

HRID 520312Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 520312
[Cl-].[Cl-].[Cl-].[Al+3].[Br:5][C:6]1[CH:14]=[CH:13][C:9]([C:10](Cl)=[O:11])=[C:8]([F:15])[CH:7]=1.[Cl:16][CH2:17][CH2:18]Cl>>[Br:5][C:6]1[CH:14]=[CH:13][C:9]([C:10](=[O:11])[CH2:18][CH2:17][Cl:16])=[C:8]([F:15])[CH:7]=1

Komponenten

4

Edukt 3

HCID 111,2-Dichloroethane2×HCID 27340264-Bromo-2-fluorobenzoyl chlorideHCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 594738271-(4-Bromo-2-fluorophenyl)-3-chloro-1-propanoneAusbeute 68 %

Versuchsvorschrift

To a stirred suspension of aluminum trichloride (153 g, 1.15 mol) in DCE (1000 mL) was added a solution of 144b (271 g, 1.14 mol) in DCE (1000 mL) at 0° C. See FIG. 3. Ethylene gas was bubbled through the dark suspension for 3 h until the acid chloride was consumed. The reaction mixture was then stirred at RT overnight, cooled to 0° C., and quenched with 4M HCl (500 mL). The organic phase was separated and washed with brine (100 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude residue was purified by column chromatography (PE/EA=30 to 10:1) to give 1-(4-bromo-2-fluorophenyl)-3-chloropropan-1-one 144c (210 g, 68%).

Aufarbeitung

  1. customEthylene gas was bubbled through the dark suspension for 3 h until the acid chloride
  2. customwas consumed
  3. temperaturecooled to 0° C.
  4. customquenched with 4M HCl (500 mL)
  5. customThe organic phase was separated
  6. washwashed with brine (100 mL)
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customThe crude residue was purified by column chromatography (PE/EA=30 to 10:1)

Quellen und Nachweise

ORD-Eintrag
ord-9946ceff88c245b994c6a22182dd4693
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09326985B2

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