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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891807Generated: October 29, 2026

3-t-Butyldiphenylsilyloxy-1-(4-hydroxymethyl-1,3-oxazol-2-yl)azetidine → 3-t-Butyldiphenylsilyloxy-1-(4-formyl-1,3-oxazol-2-yl)azetidine

https://huagongshe.com/reaction/891807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-t-Butyldiphenylsilyloxy-1-(4-hydroxymethyl-1,3-oxazol-2-yl)azetidineHCID 22242815—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product3-t-Butyldiphenylsilyloxy-1-(4-formyl-1,3-oxazol-2-yl)azetidineHCID 2224272180%

Reaction Steps

To a solution of 3-t-butyldiphenylsilyloxy-1-(4-hydroxymethyl-1,3-oxazol-2-yl)azetidine (3.88 g, 9.50 mmol) (obtained as described in Reference Example 70(9)) in methylene chloride (190 ml) was added activated manganese dioxide (19.4 g) and the mixture was stirred at room temperature for 2 hours. After checking the completion of the reaction, the mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (3:1) as the eluant to afford 3-t-butyldiphenylsilyloxy-1-(4-formyl-1,3-oxazol-2-yl)azetidine (3.09 g, yield 80%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-7229c60397f84343a5f55271ce796ad5
Source noteuspto-grants-2006_02