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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425514Generated: October 30, 2026

6-(Benzyloxy)-3,3-dimethyl-2,3-dihydrobenzofuran → 3,3-Dimethyl-2,3-dihydro-1-benzofuran-6-ol

https://huagongshe.com/reaction/425514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Benzyloxy)-3,3-dimethyl-2,3-dihydrobenzofuranHCID 66642617—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3,3-Dimethyl-2,3-dihydro-1-benzofuran-6-olHCID 2148521974%

Reaction Steps

To a solution of 6-(benzyloxy)-3,3-dimethyl-2,3-dihydrobenzofuran (3.48 g, 13.7 mmol) in methanol (200 mL) was added Pd/C (1.45 g) and the mixture was hydrogenated under 40 psi of hydrogen overnight. The reaction mixture was filtered through celite, washed with methanol. The filtrate was concentrated in vacuo to dryness. The residue was subjected to column chromatography (ethyl acetate/hexane, 1/7) to give the title compound (1.66 g, 74%): MS (ES+) m/z 165.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106087B2
Source datasetuspto-grants-2012_01
ORD IDord-2446f4df1b7a4a22abc0ea809cfba3c5
Source noteuspto-grants-2012_01