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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030873Generated: October 31, 2026

4-tert-Butylcyclohexanone → 4-tert-Butylcyclohexanol

https://huagongshe.com/reaction/1030873

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylcyclohexanoneHCID 7392—
ReactantHCID 178418361HCID 178418361—
SolventCyclohexaneHCID 8078—
Product4-tert-ButylcyclohexanolHCID 739193.8%

Reaction Steps

A mixture composed of 100 g (0.649 mole) of 4-tert-butyl-cyclohexanone, 1.35 g of the catalyst prepared as indicated in Example 1 and 150 g of cyclohexane were put into an autoclave under nitrogen and then hydrogen was introduced until the pressure settled at about 106Pa. The mixture was then heated to 70° and the reaction was followed by gas chromatography. The reaction was stopped by cooling and the autoclave was flushed with nitrogen. After filtering, the catalyst was recovered under argon flow, washed with cyclohexane and recycled for the following hydrogenation operations. The clear filtrate was evaporated to give a residue that, once distilled, provided 95.15 g of an isomeric mixture containing 87.7% of cis isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05107038
Source datasetuspto-grants-1992_04
ORD IDord-4425fc7e446244b1aac43171a41a127d
Source noteuspto-grants-1992_04