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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879558Generated: October 30, 2026

2-(4-(benzyloxy)-3-(methoxymethoxy)phenyl)-3,7-bis(methoxymethoxy)-4H-chromen-4-one → 2-(4-hydroxy-3-(methoxymethoxy)phenyl)-3,7-bis(methoxymethoxy)-4H-chromen-4-one

https://huagongshe.com/reaction/1879558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(benzyloxy)-3-(methoxymethoxy)phenyl)-3,7-bis(methoxymethoxy)-4H-chromen-4-oneHCID 66933930—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(4-hydroxy-3-(methoxymethoxy)phenyl)-3,7-bis(methoxymethoxy)-4H-chromen-4-oneHCID 6693409399.6%

Reaction Steps

To 2-(4-(benzyloxy)-3-(methoxymethoxy)phenyl)-3,7-bis(methoxymethoxy)-4H-chromen-4-one (55 mg, 0.108 mmol) in 10 mL MeOH was added Palladium on activated carbon (20 mg). The mixture was stirred at rt under H2 atmosphere for 2 h. Solid was filtered off and the filtrate was concentrated to afford 2-(4-hydroxy-3-(methoxymethoxy)phenyl)-3,7-bis(methoxymethoxy)-4H-chromen-4-one as a yellow solid (45 mg, 99%). This material was used directly for the next reaction without purification. MS (ESI) m/z 419 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318132B2
Source datasetuspto-grants-2012_11
ORD IDord-11c2c8d2a8cd46c5b67221b238713980
Source noteuspto-grants-2012_11