HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1,1-Dimethoxycyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Isobutanol | HCID 6560 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Product | 1,1-Dimethoxycyclohexane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399778 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-7494e292c8174cdd8b0415f471985ec2 |
| Source note | uspto-grants-1995_03 |