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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrapropylammonium | HCID 9559 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 1-(2-{[Tert-butyl(dimethyl)silyl]oxy}ethyl)-1h-pyrazole-3,5dimethanol | HCID 21941467 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-([tert-butyl(dimethyl)silyl]oxy}ethyl)-1H-pyrazole-3,5-dicarbaldehyde | HCID 86607968 | 69.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112582B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-4ab526f3692e48e7bf5315974db91633 |
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| Source note | uspto-grants-2006_09 |
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