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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881932Generated: October 27, 2026

[5-({[Tert-butyl(diphenyl)silyl]oxy}methyl)-1,3,4-thiadiazol-2-yl]methanol → 5-({[Tert-butyl(diphenyl)silyl]oxy}methyl)-1,3,4-thiadiazole-2-carbaldehyde

https://huagongshe.com/reaction/1881932

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[5-({[Tert-butyl(diphenyl)silyl]oxy}methyl)-1,3,4-thiadiazol-2-yl]methanolHCID 59331609—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product5-({[Tert-butyl(diphenyl)silyl]oxy}methyl)-1,3,4-thiadiazole-2-carbaldehydeHCID 5933162671%

Reaction Steps

To a solution of [5-({[tert-butyl(diphenyl)silyl]oxy}methyl)-1,3,4-thiadiazol-2-yl]methanol (242 mg) in toluene (2 mL) was added manganese dioxide (693 mg), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated to give the title compound (171 mg) as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-20ad57e2cdbe488098195c30815b7055
Source noteuspto-grants-2012_11