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Benzene → 4-Bromo-2-fluoro-1,1'-biphenyl

HRID 326027
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 326027
N(OCCC(C)C)=O.[Br:9][C:10]1[CH:16]=[CH:15][C:13](N)=[C:12]([F:17])[CH:11]=1.[CH:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>Cl.O.[Zn].[Fe]>[Br:9][C:10]1[CH:16]=[CH:15][C:13]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[C:12]([F:17])[CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 241Benzene2×HCID 8053Isoamyl NitriteHCID 1230504-Bromo-2-fluoroaniline

Produkt 1

HCID 5210634-Bromo-2-fluoro-1,1'-biphenyl

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 23925IronKatalysatorHCID 23994ZincKatalysator
HCID 313
Hydrochloric Acid
Lösungsmittel
HCID 962WaterLösungsmittel

Versuchsvorschrift

Solutions of 375 ml (325 g, 2.8 moles) of isoamyl nitrite, and of 378 grams (2.0 moles) of crude 4-bromo-2-fluoroaniline in 250 ml benzene are added separately and simultaneously dropwise over about 20 hours to 3500 ml of benzene vigorously stirred under a nitrogen atmosphere, and kept in a water bath at 65° C. The mixture is kept overnight at 65° C., then cooled, washed twice with 250 ml of water and evaporated. The dark oily residue is dissolved in 750 ml methanol and 450 ml concentrated hydrochloric acid, and treated with 138 grams (2.1 moles) of granular zinc, added in small portions over about 6 hours. In order to complete this "reductive upgrading", the solution is treated with 54 grams (1.0 mole) of fine iron filings over 0.5 hours. Within one hour the color of the mixture is visibly lighter. The solution is diluted with one liter of water and one liter of Skellysolve B hexanes, and the liquids are decanted from the remaining metals. The aqueous phase is extracted twice with one liter of Skellysolve B hexanes and the one liter of water, one liter of 1 N NaOH, and one liter of water. The solution is then passed through anhydrous sodium sulfate and evaporated to provide 389 grams of 4-bromo-2-fluoro-biphenyl.

Aufarbeitung

  1. customkept in a water bath at 65° C
  2. temperaturecooled
  3. washwashed twice with 250 ml of water
  4. customevaporated
  5. dissolutionThe dark oily residue is dissolved in 750 ml methanol
  6. additionadded in small portions over about 6 hours
  7. waitWithin one hour the color of the mixture is visibly lighter
  8. customthe liquids are decanted from the remaining metals
  9. extractionThe aqueous phase is extracted twice with one liter of Skellysolve B hexanes
  10. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-601a58a21c684548beb39da1256352bc
Quelldatensatz
uspto-grants-1984_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04443631

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