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N-bromobutanimide → 3-Bromo-2-chloro-6-fluorobenzonitrile

HRID 2175864
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2175864
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[C:4]#[N:5].C1C(=O)N([Br:18])C(=O)C1>>[Br:18][C:9]1[C:2]([Cl:1])=[C:3]([C:6]([F:10])=[CH:7][CH:8]=1)[C:4]#[N:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 67184N-bromobutanimideHCID 695872-Chloro-6-fluorobenzonitrile

Produkt 1

HCID 712393913-Bromo-2-chloro-6-fluorobenzonitrile

Versuchsvorschrift

2-Chloro-6-fluorobenzonitrile (15.6 g, 100 mmol) was dissolved in trific acid (75 mL) at 0° C., then NBS (17.8 g, 100 mmol) was added. The reaction was warmed up to room temperature and stirred overnight. The reaction mixture was poured into ice and extracted with DCM (2×). DCM layers were washed with NaHCO3 and brine. The DCM was dried over Na2SO4 then filtered and concentrated. The product was purified by chromatography through a 330 g ISCO Redi-Sep column with 10-20% ethyl acetate/hexane solvent system to yield 3-bromo-2-chloro-6-fluorobenzonitrile.

Aufarbeitung

  1. additionThe reaction mixture was poured into ice
  2. extractionextracted with DCM (2×)
  3. washDCM layers were washed with NaHCO3 and brine
  4. dry with material
Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion
The DCM was dried over Na2SO4
  • filtrationthen filtered
  • concentrationconcentrated
  • customThe product was purified by chromatography through a 330 g ISCO Redi-Sep column with 10-20% ethyl acetate/hexane solvent system
  • Quellen und Nachweise

    ORD-Eintrag
    ord-cd30bb8eace2482caa410581cb2ed420
    Quelldatensatz
    uspto-grants-2015_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US09062070B2

    Notizen zur Reaktion

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