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Pyridine → 3-Acetyl-4-fluorobenzonitrile

HRID 398358
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 398358
N1C=CC=CC=1.[F:7][C:8]1[CH:15]=[CH:14][C:11]([C:12]#[N:13])=[CH:10][C:9]=1[CH:16]([OH:18])[CH3:17]>C(Cl)Cl.CCOCC.[O-2].[O-2].[O-2].[Cr+6]>[C:12]([C:11]1[CH:14]=[CH:15][C:8]([F:7])=[C:9]([C:16](=[O:18])[CH3:17])[CH:10]=1)#[N:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 1049PyridineHCID 230001664-Fluoro-3-(1-hydroxyethyl)benzonitrile

Produkt 1

HCID 230002093-Acetyl-4-fluorobenzonitrile

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 10219390chromium (VI) trioxideKatalysatorHCID 3283Diethyl EtherLösungsmittelHCID 6344
Dichloromethane
Lösungsmittel
2×

Versuchsvorschrift

To a solution of pyridine (3.52 mL, 43.6 mmol) in CH2Cl2 (10 mL) was added dry chromium trioxide (2.18 g, 21.80 mmol) at 0° C. The reaction mixture was warmed to room temperature and stirred for 30 min. 4-fluoro-3-(1-hydroxyethyl)benzonitrile (600 mg, 3.63 mmol) dissolved in CH2Cl2 (10 mL) was added via canula. The reaction mixture was stirred for 10 min. and was diluted with ether and celite and stirred for an additional 20 min. The reaction mixture was filtered through a pad of celite and washed with ethyl acetate. The organic was washed then with 5% HCl and sat'd NaHCO3, brine, dried over MgSO4, and concentrated in vacuo to provide product:

Aufarbeitung

  1. additionwas added via canula
  2. stirringThe reaction mixture was stirred for 10 min.
  3. stirringstirred for an additional 20 min
  4. filtrationThe reaction mixture was filtered through a pad of celite
  5. washwashed with ethyl acetate
  6. washThe organic was washed
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated in vacuo
  9. customto provide product

Quellen und Nachweise

ORD-Eintrag
ord-038e7fabcbb3469f8fbe081927318655
Quelldatensatz
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06610692B1

Notizen zur Reaktion

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