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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974772Generated: October 26, 2026

Aniline → N-Cyclohexylaniline

https://huagongshe.com/reaction/1974772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantNitrobenzeneHCID 7416—
ReactantCyclohexanolHCID 7966—
ReactantCyclohexanoneHCID 7967—
ReactantN-cyclohexylideneanilineHCID 315516—
CatalystZinc AcetateHCID 11192—
ProductN-CyclohexylanilineHCID 74567—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283365
Source datasetuspto-grants-1994_02
ORD IDord-9616a9f5c7534990bc5573bcffaf83b7
Source noteuspto-grants-1994_02