HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268306Generated: October 30, 2026
Methyl morpholine oxide → 1alpha,3beta-Bis(tert-butyldimethylsilyloxy)-20-oxopregna-5,7,16-triene
https://huagongshe.com/reaction/2268306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 1alpha,3beta-bis(tert-butyldimethylsilyloxy)-20(S)-hydroxypregna-5,7,16-triene | HCID 12020078 | — |
| Catalyst | HCID 178449048 | HCID 178449048 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1alpha,3beta-Bis(tert-butyldimethylsilyloxy)-20-oxopregna-5,7,16-triene | HCID 12020082 | 74.5% |
Reaction Steps
A solution of 1α,3β-bis(tert-butyldimethylsilyloxy)-20(S)-hydroxypregna-5,7,16-triene (50.0 mg, 0.0894 mmol) and 4-methylmorpholine-N-oxide (15.7 mg, 0.134 mmol) in dichloromethane (1 ml) was stirred with powdered molecular sieve 4A at room temperature for 10 minutes. This was combined with tetra-n-butylammonium perruthenate (1.6 mg, 0.00447 mmol) and stirred at room temperature for 30 minutes. The reaction solution was filtered and then diluted with dichloromethane, and the organic layer was washed with saturated aqueous sodium bicarbonate solution, brine and saturated aqueous copper sulfate solution successively and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by preparative thin layer chromatography (0.5 mm×1, hexane:ethyl acetate=5:1, developed once) to give the title compound as a colorless solid (37.1 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326503B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-a992f325f0cd47ab97432d3e18a8f9e2 |
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| Source note | uspto-grants-2001_12 |
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