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  2. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide -based reagents used as accelerators for vulcanization. It is a building block for pharmaceuticals (e.g., mucolytics, analgesics, and bronchodilators ).

  3. Arylcyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Arylcyclohexylamine

    History. Phencyclidine (PCP) is believed to be the first arylcyclohexylamine with recognized anesthetic properties, but several arylcyclohexylamines were described before PCP in the scientific literature, beginning with PCA (1-phenylcyclohexan-1-amine) the synthesis of which was first published in 1907. PCP itself was discovered in 1926 but not ...

  4. Eticyclidine - Wikipedia

    en.wikipedia.org/wiki/Eticyclidine

    Eticyclidine ( PCE, CI-400) is a dissociative anesthetic drug with hallucinogenic effects. It is similar in effects to phencyclidine but is slightly more potent. PCE was developed by Parke-Davis in the 1970s and evaluated for anesthetic potential under the code name CI-400, [2] but research into PCE was not continued after the development of ...

  5. Dicyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Dicyclohexylamine

    Synthesis. Dicyclohexylamine, as a mixture with cyclohexylamine, is prepared by the catalytic hydrogenation of aniline (phenylamine), with a catalyst of ruthenium and/or palladium. This method produces mainly cyclohexylamine with little dicyclohexylamine.

  6. Ei mechanism - Wikipedia

    en.wikipedia.org/wiki/Ei_mechanism

    The pyrolysis of N,N-dimethyl-2-phenylcyclohexylamine-N-oxide shows how conformational effects and the stability of the transition state affect product composition for cyclic substrates. In the trans isomer, there are two cis-β-hydrogens that can eliminate. The major product is the alkene that is in conjugation with the phenyl ring, presumably ...

  7. Phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Phenethylamine

    Synthesis. One method for preparing β-phenethylamine, set forth in J. C. Robinson and H. R. Snyder's Organic Syntheses (published 1955), involves the reduction of benzyl cyanide with hydrogen in liquid ammonia, in the presence of a Raney-Nickel catalyst, at a temperature of 130 °C and a pressure of 13.8 MPa. Alternative syntheses are outlined ...

  8. Phenylethanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylethanolamine

    Synthesis. An early synthesis of phenylethanolamine was by the reduction of 2-nitro-1-phenyl-ethanol. Other early syntheses are summarized in a paper by Hartung and Munch. A more recent synthesis, providing a better yield, is by the reduction of benzoyl cyanide using LiAlH 4. Properties

  9. Chemical synthesis - Wikipedia

    en.wikipedia.org/wiki/Chemical_synthesis

    A chemical synthesis involves one or more compounds (known as reagents or reactants) that will experience a transformation when subjected to certain conditions. Various reaction types can be applied to formulate a desired product.

  10. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    Ether synthesis by reaction of salicylaldehyde with chloroacetic acid and sodium hydroxide. The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol . This reaction was developed by Alexander Williamson in 1850.

  11. Phenylacetone - Wikipedia

    en.wikipedia.org/wiki/Phenylacetone

    Synthesis. There are many routes to synthesize phenylacetone. Industry uses the gas-phase ketonic decarboxylation of phenylacetic acid using acetic acid over a ceria-alumina solid acid catalyst. A related laboratory-scale reaction has been described. An alternative route is zeolite-catalyzed isomerization of phenylpropylene oxide.