HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1-(1,1-Dimethoxyethyl)-4-(4,4-dimethylcyclohex-1-enyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 1-[4-(4,4-Dimethylcyclohex-1-enyl)phenyl]ethanone | HCID 18402502 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 1-(1,1-Dimethoxyethyl)-4-(4,4-dimethylcyclohex-1-enyl)benzene | HCID 18402499 | — |
Reaction Steps
36.13 g of 1-[4-(4,4-dimethylcyclohex-1-enyl)phenyl]ethanone (compound VI.1) in 250 ml of methanol are stirred for 12 hours at room temperature in the presence of 0.5 g of para-toluenesulphonic acid (PTSA) and 13 ml of trimethyl-ortho-formate. The solvents are partially evaporated off under reduced pressure. A 50% solution of potassium hydroxide in methanol is added and the solvents are then evaporated off under reduced pressure. The residue obtained is taken up in diisopropyl ether and the solvent is then evaporated off under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06482986B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-d08d0d730ca64722896b6e9b3405be46 |
| Source note | uspto-grants-2002_11 |