HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → (4,4-Diethoxycyclohexylmethoxymethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Cyclohexanone, 4-[(phenylmethoxy)methyl]- | HCID 10443381 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4,4-Diethoxycyclohexylmethoxymethyl)benzene | HCID 57617622 | — |
Reaction Steps
4-Benzyloxymethylcyclohexanone (168 g, 0.77 mol) is dissolved in ethanol (2000 mL), and then triethylorthoformate (350 mL) and p-toluenesulfonic acid (13.3 g) are added. The resulting mixture is stirred and refluxed for 6 hours. After addition of triethylamine (10.5 mL) at room temperature, the mixture is concentrated (500 mL). After addition of sat. NaHCO3 aq., the resulting mixture is extracted with EtOAc. The water layer is extracted with EtOAc and the combined organic layer is washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The crude mixture is purified by short pad silica gel column chromatography to afford (4,4-diethoxycyclohexylmethoxymethyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410275B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-289efcd4649d4d9597efd4258cad4e7e |
| Source note | uspto-grants-2013_04 |