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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655653Generated: October 26, 2026

3-Methoxy-2-methoxymethoxy-5-(2-oxo-oxazolidin-3-yl)benzaldehyde → 3-(3-Methoxy-4-methoxymethoxy-5-methylphenyl)oxazolidin-2-one

https://huagongshe.com/reaction/655653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-2-methoxymethoxy-5-(2-oxo-oxazolidin-3-yl)benzaldehydeHCID 57482553—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product3-(3-Methoxy-4-methoxymethoxy-5-methylphenyl)oxazolidin-2-oneHCID 57499573—

Reaction Steps

3-Methoxy-2-methoxymethoxy-5-(2-oxo-oxazolidin-3-yl)benzaldehyde (0.5 g, 1.79 mmol) was dissolved in a solvent mixture of acetic acid (5 ml) and ethanol (5 ml) and 10% palladium carbon (0.05 g) was added thereto to perform catalytic reduction at 1 atm at 50° C. for 4 hours. The reaction mixture was cooled to room temperature and filtrated by cerite. The filtrate was concentrated under reduced pressure. The residue was dissolved in acetic acid (10 ml) and 10% palladium carbon (0.05 g) was added thereto to perform catalytic reduction at 1 atm at 50° C. for 6 hours. The solvent was removed under reduced pressure to obtain 3-(3-methoxy-4-methoxymethoxy-5-methylphenyl)oxazolidin-2-one as a crude product, which was subjected to the next reaction as it was.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071600B2
Source datasetuspto-grants-2011_12
ORD IDord-aa77d31e260040ff9924ee1a7a8fb23a
Source noteuspto-grants-2011_12