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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65800Generated: October 26, 2026

Carbon Dioxide → 2,3,6-Trimethylphenol

https://huagongshe.com/reaction/65800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant2-Cyclohexen-1-one, 2,5,6-trimethyl-HCID 89264—
Reactant2,3,6-Trimethylcyclohex-2-en-1-oneHCID 3016843—
ReactantTrimethyl-2-cyclohexen-1-oneHCID 13360364—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product2,3,6-TrimethylphenolHCID 1701695%

Reaction Steps

Dehydrogenation may be carried out in an inert solvent. It is advantageous however to dehydrogenate the 2,5,6-trimethyl-2-cyclohexen-1-one or 2,3,6-trimethyl-2-cyclohexen-1-one in the gas phase, for example by passing it as a gas at the dehydrogenation temperature over a palladium/silica gel catalyst. In gas-phase dehydrogenation the trimethyl-2-cyclohexen-1-one is preferably passed over the catalyst in admixture with an extraneous gas such as nitrogen, steam, carbon dioxide and particularly hydrogen; generally a ratio by volume of extraneous gas to gaseous trimethyl-2-cyclohexen-1-one of from about 1:2 to 5:1 is chosen. Temperatures of from 200° to 400° C., preferably from 250° to 350° C., are usually used in gas-phase dehydrogenation. The time that the trimethyl-2-cyclohexen-1-one is in contact with the catalyst is generally from half to fifty, preferably from two to ten seconds. The 2,3,6-trimethylphenol is obtained in a more than 95% yield in gas-phase dehydrogenation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04128728
Source datasetuspto-grants-1978_12
ORD IDord-4aab1458444845a2a8ad075eb5623b03
Source noteuspto-grants-1978_12