Water → HCID 54066355, Verbindung

HRID 1758262Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1758262
I[CH:2]([CH3:4])[CH3:3].[O:5]1[C:9]2[CH:10]=[C:11]([CH2:14][C:15]#[N:16])[CH:12]=[CH:13][C:8]=2[CH:7]=[CH:6]1.[OH-].[Na+].O>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.ClCCl>[CH:2]([CH:14]([C:11]1[CH:12]=[CH:13][C:8]2[CH:7]=[CH:6][O:5][C:9]=2[CH:10]=1)[C:15]#[N:16])([CH3:4])[CH3:3]

Komponenten

7

Versuchsvorschrift

2-Iodopropane (6.5 g, 0.038 mol) was added to a well-stirred mixture of benzofuran-6-acetonitrile (3.0 g, 0.019 mol), tetrabutylammonium hydrogen sulphate (6.5 g, 0.019 mol), sodium hydroxide (47% w/w, 20 cm3, 0.037 mol), water (10 cm3) and dichloromethane (50 cm3), and the mixture was refluxed for 6 hr. with good stirring. The organic layer was washed with water, dried (Na2SO4), filtered and the solvent was removed. Toluene (15 cm3) was added to the residue, the mixture was filtered, and the solvent was removed. The residue was chromatographed on silica using toluene as eluant, to give α-isopropylbenzofuran-6-acetonitrile (1.62, 0.0081 mol, 42.6%) as an oil. (Found: C, 79.32; H, 6.22; N, 6.55. C13H13NO requires C, 78.36, H, 6.58; N, 7.03%) t.l.c./silica/toluene RF 0.38.

Aufarbeitung

  1. temperaturethe mixture was refluxed for 6 hr
  2. washThe organic layer was washed with water
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. customthe solvent was removed
  6. additionToluene (15 cm3) was added to the residue
  7. filtrationthe mixture was filtered
  8. customthe solvent was removed
  9. customThe residue was chromatographed on silica

Quellen und Nachweise

ORD-Eintrag
ord-0dfbde7671db48dbb59306d752066a6f
Quelldatensatz
uspto-grants-1983_02
Patentnummer
US04372970

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