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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609385Generated: October 30, 2026

p-Toluenesulfonic acid → 1,1-Dimethoxycyclohexane

https://huagongshe.com/reaction/1609385

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantIsobutanolHCID 6560—
ReactantCyclohexanoneHCID 7967—
ReactantTrimethyl orthoformateHCID 9005—
Product1,1-DimethoxycyclohexaneHCID 13616—

Reaction Steps

Cyclohexanone dimethyl ketal (CHMK) was prepared as described in Example 1 from 1 mol of cyclohexanone and trimethyl orthoformate. 370.6 g of isobutanol (2-methyl-1-propanol, 5.0 mols) were added, and the transketalization was then carried out under reflux while the sump temperature was gradually increased from 110° to 160° C. After a running time of 2 hours, another 0.4 g of p-toluenesulfonic acid was added. The low-boiling-point components, i.e. methyl formate, methanol and a small amount of isobutyl formate, were removed by distillation under reflux (ratio 1:5 to 1:2) over the course of 4 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399778
Source datasetuspto-grants-1995_03
ORD IDord-7494e292c8174cdd8b0415f471985ec2
Source noteuspto-grants-1995_03