Reaction #63198

ord-477c120a9e8a486db0eedc03694403ae

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherto give a dark red coloured solution
  2. 2
    Otherquenched with ammonium chloride (20 g)
  3. 3
    Otherto evaporate
  4. 4
    Otherthe residues were partitioned between chloroform and water
  5. 5
    Extractionextracted with chloroform
  6. 6
    Dryingthe chloroform extracts were dried
  7. 7
    Otherevaporated
  8. 8
    workup.DISTILLATIONdistilled

Procedure

5,6,7,8-Tetrahydroquinoline (20 g) was added quickly to sodamide (17.6 g) in liquid ammonia (250 ml) to give a dark red coloured solution. 3-Chloropropylamine hydrochloride (28.9 g) was added in portions over four hours when loss of colour was permanent after which the reaction was stirred for a further 2 hours and then quenched with ammonium chloride (20 g). The liquid ammonia was allowed to evaporate and the residues were partitioned between chloroform and water. The pH was lowered to 6 and the chloroform layer was discarded. The aqueous layer was basified (pH 12-14), and extracted with chloroform, the chloroform extracts were dried, combined, evaporated and the residue was vacuum distilled to give 3-(5,6,7,8-tetrahydroquinol-8-yl) propylamine (7.58 g), b.p. 92°-94° C. at 0.1 mm Hg.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04764519uspto-grants-1988_08