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      • Example: Synthesis of PCE (N-ethyl-1-phenylcyclohexylamine): A mixture of 100 g of anhydrous ethylamine and 220 g of cyclohexanone was kept 16 hours, then shaken with solid KOH. The lower oil layer, which comprises the imine ( N-cyclohexylidenethylamine), was then removed by decantation.
      chemistry.mdma.ch/hiveboard/rhodium/pcp/imine_synth.html

      Reaction Scheme III. Synthesis via imines:

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  3. pubchem.ncbi.nlm.nih.gov › 1-phenylcyclohexylamine1-Phenylcyclohexylamine | C12H17N - PubChem

    1-Phenylcyclohexylamine | C12H17N | CID 31862 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological ...

    • C12H17N
    • 31.9K
    • 175.27

  4. pubchem.ncbi.nlm.nih.gov › 4-Phenylcyclohexylamine4-Phenylcyclohexylamine | C12H17N - PubChem

    4-Phenylcyclohexylamine | C12H17N | CID 29897 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological ...

    • C12H17N
    • 29.9K

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  6. www.sciencedirect.com › science › articlePhenylcyclohexylamine: Effect of a metabolite of ...

    Dec 01, 1986 · The effect of phenylcyclohexylamine (PCA) on the efflux of dopamine (DA) in the neostriatum was examined using in vivo electrochemical techniques. Phe…

    • H. Takeda, R.A. Gazzara, S.G. Howard
    • 1986

  7. erowid.org › archive › rhodiumPCP analogs via imine intermediates - Erowid

    Example: Synthesis of PCE (N-ethyl-1-phenylcyclohexylamine): A mixture of 100 g of anhydrous ethylamine and 220 g of cyclohexanone was kept 16 hours, then shaken with solid KOH. The lower oil layer, which comprises the imine ( N-cyclohexylidenethylamine), was then removed by decantation.

  8. chemistry.mdma.ch › hiveboard › rhodium-Phenylcycloalkylamine Derivatives. II.',2 Synthesis and ...

    1-Dimethylaminocyclopentyl Phenyl Ketone ( 19).13 --TU a solution of PhId (from 118 g of PhBr and 10 g of I,i in 400 ml of EtyO) was added 34.5 g (0.25 mole) of 31 in 100 ml of I<;t?O and heated 1 hr. The resultant solution was filtered through glass wool and cautiously treated with cold, diluted HC1. The amine was liberated and distilled.

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