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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189727Generated: October 31, 2026

p-Toluenesulfonic acid → Cyclohexanone, 3,3-dimethyl-

https://huagongshe.com/reaction/1189727

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantDimedoneHCID 31358—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
ProductCyclohexanone, 3,3-dimethyl-HCID 76322—

Reaction Conditions

Temperature85 °C

Reaction Steps

9.260 g of 5% Pd/C were placed in a 2 L glass-steel autoclave with glass-liner. 65 g of dimedone, 146 mL of isopropanol and 2.580 g of p-toluene sulfonic acid were added. The glass-liner was closed and stirring was started with 500 rpm. The autoclave was flushed three times with 5 bara N2. The stirrer was turned off and the autoclave was pressurized with 5 bara H2 for 10 minutes for pressure check. The pressure was released. The stirrer was turned on again to 500 rpm and the autoclave was heated to 85° C. internal temperature. The autoclave was pressurized with 2 bara H2 and the stirrer was set to 1000 rpm. The reaction mixture was stirred under 2 bara H2 at 85° C. until 123% of the theoretical H2-amount had been consumed. Then stirring was slowed to 500 rpm, the autoclave was cooled to an internal temperature below 25° C. and depressurized. After three times flushing with N2 at 5 bara for 100 minutes stirring was stopped and the autoclave was opened. The content was sucked and filtrated over a 0.45 μm filter. A 30 mL filtrated sample was diluted with 1 mL of isopropanol and 5 mg of NaHCO3 and then analyzed by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674143B2
Source datasetuspto-grants-2014_03
ORD IDord-5edf2a96c27f49faad9c38f5e5b1999b
Source noteuspto-grants-2014_03