Reaktion #684947

ord-63e429487d474d50b8f9c5f09af3289a

Reaktionsgleichung

CCCCc1ccc(CCl)cc1
4-n-butylbenzylchloride
CN(C)C=O
dimethylformamide
[H-].[Na+]
sodium hydride
CN(C)C=O
dimethylformamide
N#CC1c2ccccc2C=CN1C(=O)c1ccccc1
1-cyano-2-benzoyl-1,2-dihydroisoquinoline
CCCCc1ccc(Cc2nccc3ccccc23)cc1
aforementioned compound
Ausbeute 17.2%
CCCCc1ccc(Cc2nccc3ccccc23)cc1
1-(4-butylbenzyl)isoquinoline
Ausbeute 17.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthis was concentrated
  2. 2
    workup.ADDITIONtoluene and water were added to this residue
  3. 3
    WaschenThe toluene layer was washed with water
  4. 4
    Trocknendried over potassium carbonate
  5. 5
    Einengenconcentrated
  6. 6
    workup.ADDITIONTo an ethanol (1.6 ml) solution of the residue, 50% aqueous sodium hydroxide solution (0.63 ml) was added
  7. 7
    Temperaturthis was refluxed for 2 hours
  8. 8
    EinengenAfter concentration, toluene and water
  9. 9
    workup.ADDITIONwere added
  10. 10
    WaschenThe toluene layer was washed with water
  11. 11
    Trocknendried over calcium carbonate
  12. 12
    Einengenconcentrated
  13. 13
    SonstigeThe residue was purified by silica gel column chromatography

Vorschrift

To a dimethylformamide (1.8 ml) solution of 60% sodium hydride (16 mg, 0.40 mmol), a dimethylformamide (3.6 ml) solution of 1-cyano-2-benzoyl-1,2-dihydroisoquinoline (100 mg, 0.38 mmol) synthesized according to the literature of Org. Synth., VI, 115 (1988), and 4-n-butylbenzylchloride (70 mg, 0.38 mmol) was added dropwise under nitrogen atmosphere at −16° C., and was further stirred at room temperature for 30 minutes. Water was added, this was concentrated, and toluene and water were added to this residue. The toluene layer was washed with water, dried over potassium carbonate, and concentrated. To an ethanol (1.6 ml) solution of the residue, 50% aqueous sodium hydroxide solution (0.63 ml) was added, and this was refluxed for 2 hours. After concentration, toluene and water were added. The toluene layer was washed with water, then dried over calcium carbonate, and then concentrated. The residue was purified by silica gel column chromatography to give 18 mg of the aforementioned compound of the formula (Ia).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07897387B2uspto-grants-2011_03