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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methoxy-2-methoxymethoxy-5-(2-oxo-oxazolidin-3-yl)benzaldehyde | HCID 57482553 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(3-Methoxy-4-methoxymethoxy-5-methylphenyl)oxazolidin-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071600B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-aa77d31e260040ff9924ee1a7a8fb23a |
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| Source note | uspto-grants-2011_12 |
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