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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261337Generated: November 2, 2026

(5-Tert-butyl-1,2-oxazol-3-yl)methanol → 5-(Tert-butyl)isoxazole-3-carbaldehyde

https://huagongshe.com/reaction/2261337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Tert-butyl-1,2-oxazol-3-yl)methanolHCID 10820794—
CatalystHCID 178418406HCID 178418406—
Solvent1,4-DioxaneHCID 31275—
Product5-(Tert-butyl)isoxazole-3-carbaldehydeHCID 4508380296.8%

Reaction Steps

1.35 g of (5-t-butyl-isoxazol-3-yl)methanol was dissolved in 50 ml of 1,4-dioxane, and 6.42 g of manganese dioxide was then added. The mixture was stirred and heated under reflux for 10 hours. The reaction mixture was cooled to room temperature and then filtered through Celite®. The filtrate was concentrated under reduced pressure to obtain 1.29 g of 5-t-butyl-isoxazole-3-carbaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846956B2
Source datasetuspto-grants-2010_12
ORD IDord-56369eed634945b3b4048aaaeb3941aa
Source noteuspto-grants-2010_12