HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Phenyl-1,3-dioxan-5-yl)methanol → 2-Phenyl-1,3-dioxane-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Phenyl-1,3-dioxan-5-yl)methanol | HCID 10679342 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenyl-1,3-dioxane-5-carbaldehyde | HCID 22492879 | 26.3% |
Reaction Steps
To a solution of (2-phenyl-1,3-dioxan-5-yl)methanol (2.0 g) in dichloromethane (40 ml) were added pyridinium chlorochromate (11.6 g) and molecular seaves 4A powder (5.0 g) with stirring and the mixture was stirred at ambient temperature for 5 hours. To a reaction mixture was added dichloromethane (100 ml) and the insoluble material was filtered off with celite and the filtrates were washed in turn with water, saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo to give 2-phenyl-1,3-dioxane-5-carbaldehyde (0.52 g). This compound was immediately used as the starting compound for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884774B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-2884ad90bf6b4cf4b524fdc968bd7f49 |
| Source note | uspto-grants-2005_04 |