HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 5-Cyclohexyl-2,2-dimethyl-5-formyl-1,3-dioxane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 5-Cyclohexyl-2,2-dimethyl-5-hydroxymethyl-1,3-dioxane | HCID 19904432 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Cyclohexyl-2,2-dimethyl-5-formyl-1,3-dioxane | HCID 19904425 | — |
Reaction Steps
5-Cyclohexyl-2,2-dimethyl-5-hydroxymethyl-1,3-dioxane (2.2 g.) was added to a stirred suspension of pyridinium chlorochromate (6.1 g.) and anhydrous sodium acetate (3.0 g.) in dry dichloromethane (50 ml.), at 0°, under a current of nitrogen. The mixture was stirred at room temperature for six hours. The mixture was diluted with dry ether (100 ml) and the organic solution was decanted off. The oily residue was treated with ether and the combined extracts were evaporated in vacuo. 5-Cyclohexyl-2,2-dimethyl-5-formyl-1,3-dioxane was obtained as a pale yellow oil (1.8 g.) and was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05098929 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-0ad1f91a08484e22b0c14b4aa16c697a |
| Source note | uspto-grants-1992_03 |