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Dimethylformamide → HCID 22996206, Verbindung

HRID 1167293
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1167293
Br[C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[O:9][CH2:10][CH3:11].[CH3:12][N:13](C)C=O>C(OCC)C.C(=O)(O)[O-].[Na+].[C-]#N.[Zn+2].[C-]#N.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:10]([O:9][C:3]1[CH:4]=[CH:5][C:6]([CH3:8])=[CH:7][C:2]=1[C:12]#[N:13])[CH3:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 2

HCID 6228DimethylformamideHCID 229962372-Bromo-1-ethoxy-4-methylbenzene

Produkt 1

HCID 22996206HCID 22996206, VerbindungAusbeute 33 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 11186Zinc cyanide (Zn(CN)2)KatalysatorHCID 178418397HCID 178418397, VerbindungKatalysator
HCID 3283
Diethyl Ether
Lösungsmittel
HCID 516892Sodium BicarbonateLösungsmittel

Reaktionsbedingungen

Temperatur
95 °C

Versuchsvorschrift

To a solution of 2-bromo-1-ethoxy-4-methyl-benzene (940 mg, 4.37 mmol) in dimethylformamide (5 mL) at room temperature was added zinc cyanide (513.1 mg, 4.37 mmol). The reaction mixture was degassed by passing argon through for 2 h before tetrakis(triphenylphosphine)palladium (505 mg, 0.437 mmol) was added. The reaction mixture was heated at 90-100° C. under argon for 12 h. The slurry reaction mixture was taken up in diethyl ether (10 mL) and sodium bicarbonate solution (2 mL). The product was extracted with diethyl ether (2×30 mL). The organic layers were washed with water (1×5 mL), brine (1×5 mL) and dried over anhydrous sodium sulfate. The solid was then filtered off, and the filtrate was concentrated in vacuo. Purification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel) eluting with 10% ethyl acetate in hexanes yielded 2-ethoxy-5-methyl-benzonitrile (232 mg, 33%).

Aufarbeitung

  1. customThe reaction mixture was degassed
  2. customthrough for 2 h
  3. additionwas added
  4. customThe slurry reaction mixture
  5. extractionThe product was extracted with diethyl ether (2×30 mL)
  6. washThe organic layers were washed with water (1×5 mL), brine (1×5 mL)
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationThe solid was then filtered off
  9. concentrationthe filtrate was concentrated in vacuo
  10. customPurification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel)
  11. washeluting with 10% ethyl acetate in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-088e5a22a5284980aacb40bf6464f5a9
Quelldatensatz
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06617346B1

Notizen zur Reaktion

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