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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816356Generated: October 25, 2026

(2-Phenyl-1,3-dioxan-5-yl)methanol → 2-Phenyl-1,3-dioxane-5-carbaldehyde

https://huagongshe.com/reaction/1816356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Phenyl-1,3-dioxan-5-yl)methanolHCID 10679342—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product2-Phenyl-1,3-dioxane-5-carbaldehydeHCID 2249287926.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884774B2
Source datasetuspto-grants-2005_04
ORD IDord-2884ad90bf6b4cf4b524fdc968bd7f49
Source noteuspto-grants-2005_04