Reaction #2061954

ord-9616a9f5c7534990bc5573bcffaf83b7

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherReaction

Procedure

Reaction was carried out by the use of the same apparatus and the same procedure as in Example 1 except that zinc acetate was not employed. In this case, a distilled aniline layer contained, as impurities, 200-350 ppm of cyclohexanol, 1300-2200 ppm of cyclohexanone, 70-130 ppm of cyclohexylideneaniline and 20 ppm or less of nitrobenzene, and the purity of the aniline was merely 99.68-99.80%. Furthermore, in the liquid phase in the reactor, N-cyclohexylaniline was formed rapidly and its content reached about 1.7% after 9 hours had elapsed since the start of the reaction, although the content of nitrobenzene in this liquid phase was maintained at 0.01% or less.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05283365uspto-grants-1994_02