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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332656Generated: October 26, 2026

(3-((1,3-Dioxolan-2-yl)methyl)phenyl)methanol → 3-((1,3-Dioxolan-2-yl)methyl)benzaldehyde

https://huagongshe.com/reaction/332656

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-((1,3-Dioxolan-2-yl)methyl)phenyl)methanolHCID 86676899—
CatalystHCID 178418406HCID 178418406—
Solvent1,4-DioxaneHCID 31275—
Product3-((1,3-Dioxolan-2-yl)methyl)benzaldehydeHCID 1163697676%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of (3-((1,3-dioxolan-2-yl)methyl)phenyl)methanol (prepared as in Example 22, Step 1 with 3-((1,3-dioxolan-2-yl)methyl)benzoic acid replacing 4-((1,3-dioxolan-2-yl)methyl)benzoic acid; 0.47 g, 2.42 mmol) in 1,4-dioxane (8 mL), manganese (IV) oxide (2.35 g) was added. The resulting suspension was heated at 100° C. for 16 hours. The reaction mixture was allowed to cool, and the suspension was filtered through a pad of celite. The celite pad was washed with ethyl acetate and the filtrate evaporated at reduced pressure to afford the title compound (0.352 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877774B2
Source datasetuspto-grants-2014_11
ORD IDord-aecf4b55f3aa4ca0812ef3901afc8ad0
Source noteuspto-grants-2014_11