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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782093Generated: October 30, 2026

(5R)-3-(3-Fluoro-4-iodophenyl)-5-[(4-hydroxymethyl-1H-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one → 1-{[(5R)-3-(3-Fluoro-4-iodophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}-1H-1,2,3-triazole-4-carbaldehyde

https://huagongshe.com/reaction/1782093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5R)-3-(3-Fluoro-4-iodophenyl)-5-[(4-hydroxymethyl-1H-1,2,3-triazol-1-yl)methyl]oxazolidin-2-oneHCID 58822464—
CatalystManganese oxideHCID 160959—
Solvent1,4-DioxaneHCID 31275—
Product1-{[(5R)-3-(3-Fluoro-4-iodophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}-1H-1,2,3-triazole-4-carbaldehydeHCID 57588294—

Reaction Conditions

Temperature70 °C

Reaction Steps

(5R)-3-(3-Fluoro-4-iodophenyl)-5-[(4-hydroxymethyl-1H-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one (5.7 g, 13.6 mmol) and manganese oxide (3.56 g, 40.9 mmol) were mixed and heated up to 100° C. in dry 1,4-dioxane for 48 hours, then the mixture was cooled down to 70° C. and filtered through celite. The filtrate was concentrated and dissolved in 5% methanol in dichloromethane, hexaneses was added and the formed precipitates were filtered and collected as the title compound (3.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498350B2
Source datasetuspto-grants-2009_03
ORD IDord-5f65c6596ddf4a568c66f998d56c951f
Source noteuspto-grants-2009_03