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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
Reactant3-Tert-butylsilyloxy-3-methyl-2-methylidenebutan-1-olHCID 131725996—
CatalystHCID 178449048HCID 178449048—
SolventDichloromethaneHCID 6344—
Product2-(Tert-butyl-dimethyl-silanyloxymethyl)-propenalHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-ecfaf161a3b54a698904999a366ed1eb
Source noteuspto-grants-2009_02