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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091350Generated: October 27, 2026

[5-(Benzyloxy)-3-methyl-1-benzofuran-2-yl]methanol → 5-(Benzyloxy)-3-methyl-1-benzofuran-2-carbaldehyde

https://huagongshe.com/reaction/2091350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[5-(Benzyloxy)-3-methyl-1-benzofuran-2-yl]methanolHCID 66778297—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product5-(Benzyloxy)-3-methyl-1-benzofuran-2-carbaldehydeHCID 8666275396.4%

Reaction Steps

To a solution (30 mL) of [5-(benzyloxy)-3-methyl-1-benzofuran-2-yl]methanol (2.8 g) synthesized in the above-mentioned (2) in toluene was added manganese dioxide (5 g), and the mixture was heated under reflux with a Dean-Stark trap for 1 hr. The reaction mixture was allowed to cool to room temperature, catalyst was filtered through celite. The filtrate was concentrated under reduced pressure to give the title object compound (2.68 g, 94%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-db20419ce3e349ce9c6ad723b9299081
Source noteuspto-grants-2013_05