1-Chloromethylnaphthalene → 1-Naphthaleneacetonitrile

HRID 619349

Reaktionsgleichung

Reaktionsgleichung von HRID 619349
Cl[CH2:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=1.[C-:13]#[N:14].[K+]>CN(C=O)C.[I-].[K+]>[C:3]1([CH2:2][C:13]#[N:14])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=1

Komponenten

5

Edukt 2

HCID 68451-ChloromethylnaphthaleneHCID 9032Potassium Cyanide

Produkt 1

HCID 85961-NaphthaleneacetonitrileAusbeute 98 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 4875Potassium IodideKatalysatorHCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

1-Chloromethyinaphthalene (5.00 ml, 33 mmol) was dissolved in N,N'-dimethylformamide (50 ml) and potassium cyanide (4.31 g, 66 mmol) and potassium iodide (0.1 g) were added and the resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was partitioned between water (150 ml) and diethyl ether (2×100 ml). The combined organic phases were washed with water (100 ml), dried (MgSO4), filtered and concentrated in vacuo affording 5.41 g (98%) of 1-naphtylacetonitrile as an oil.

Aufarbeitung

  1. customThe reaction mixture was partitioned between water (150 ml) and diethyl ether (2×100 ml)
  2. washThe combined organic phases were washed with water (100 ml)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-de3f8fa39a1048f5b83f53a4b54780a8
Quelldatensatz
uspto-grants-1999_09
Patentnummer
US05958957

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