HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728039Generated: October 29, 2026
Methyl morpholine oxide → 2-(Tert-butyl-dimethyl-silanyloxymethyl)-propenal
https://huagongshe.com/reaction/1728039
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 3-Tert-butylsilyloxy-3-methyl-2-methylidenebutan-1-ol | HCID 131725996 | — |
| Catalyst | HCID 178449048 | HCID 178449048 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Tert-butyl-dimethyl-silanyloxymethyl)-propenal | HCID 131727334 | — |
Reaction Steps
2-(Tert-butyl-dimethyl-silanyloxymethyl)-prop-2-en-1-ol (6 g, 29.7 mmol) prepared in example 99a was dissolved in dichloromethane (296 mL) containing both the molecular sieves (4 A) (Aldrich) and N-methyl morpholine oxide (5.2 g, 44.47 mmol). After stirring the mixture for 1 h, (Tetra-n-butyl ammonium perruthenate) (0.47 g, 1.48 mmol) (Aldrich) was added and the reaction mixture was stirred at room temperature for 1 h. Then another batch of (Tetra-n-butyl ammonium per-ruthenate) (0.23 g, 0.74 mmol) was added and the mixture was stirred at room temperature for another 1 h. The reaction mixture was diluted with dichloromethane. The organic layer was washed with Na2S2O3 solution, brine and saturated copper (II) sulfate solution, then dried over dried over MgSO4, filtered and concentrated. The residue was purified with chromatography to give 2-(tert-butyl-dimethyl-silanyloxymethyl)-propenal to as colorless oil (Yield 1.3 g, 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07495007B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-ecfaf161a3b54a698904999a366ed1eb |
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| Source note | uspto-grants-2009_02 |
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