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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216579Generated: November 1, 2026

Tetrapropylammonium → 1-(2-([tert-butyl(dimethyl)silyl]oxy}ethyl)-1H-pyrazole-3,5-dicarbaldehyde

https://huagongshe.com/reaction/2216579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrapropylammoniumHCID 9559—
ReactantMethyl morpholine oxideHCID 82029—
Reactant1-(2-{[Tert-butyl(dimethyl)silyl]oxy}ethyl)-1h-pyrazole-3,5dimethanolHCID 21941467—
SolventDichloromethaneHCID 6344—
Product1-(2-([tert-butyl(dimethyl)silyl]oxy}ethyl)-1H-pyrazole-3,5-dicarbaldehydeHCID 8660796869.9%

Reaction Steps

To a stirred solution of 1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-1H-pyrazole-3,5-dimethanol (1.18 g, 4 mmol) in methylene chloride (20 ml), was added 4-methylmorpholine-N-oxide (2.89 g, 24 mmol) and molecular sieve 4A (4 g). The reaction mixture was stirred at room temperature for 10 min. and then treated with tetrapropylammonium peruthenate (0.15 g, 0.4 mmol). Stirring was continued for 2 hr. The methylene chloride solution was concentrated and diluted with ether (40 ml). The mixture was filtered through a pad of silica gel (40 g) and the filter pad was eluted with 2×20 ml ether. The combined eluent was washed with 1 N HCl and brine, dried over anhydrous sodium sulfate, and evaporated to give 0.79 g of a white solid; mp 63–64° C.; MS m/e 283 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112582B2
Source datasetuspto-grants-2006_09
ORD IDord-4ab526f3692e48e7bf5315974db91633
Source noteuspto-grants-2006_09