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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576493Generated: October 31, 2026

Benzenamine, 4-(phenylmethyl)- → Cyclohexanamine, 4-(cyclohexylmethyl)-

https://huagongshe.com/reaction/1576493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 4-(phenylmethyl)-HCID 136914—
ReactantPotassium methoxideHCID 23664618—
ReactantHCID 178418361HCID 178418361—
CatalystRutheniumHCID 23950—
ProductCyclohexanamine, 4-(cyclohexylmethyl)-HCID 299588—

Reaction Conditions

Temperature290 °C

Reaction Steps

In a steel autoclave fitted with a stirring apparatus and a product draw off system retaining the catalyst in the reactor can be placed 200 parts of 4-aminodiphenylmethane as described in British Patent 764,633 and 100 parts of a finely divided 5% ruthenium on an alumina support and 15 parts of potassium methoxide. The mixture within the autoclave can then be heated to 290°C with stirring and hydrogen added to maintain a pressure of 290 atmospheres for 20 minutes. The resulting mixture can then be freed of catalyst by filtration and distilled to strip off solvent. Final distillation under vacuum can then be used to provide the desired product, 4-aminodicyclohexylmethane, which is a colorless viscose liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03981766
Source datasetuspto-grants-1976_09
ORD IDord-3d9046b793864de19c3a8d98b547d81f
Source noteuspto-grants-1976_09