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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922632Generated: November 2, 2026

Methyl morpholine oxide → 1-{(E,3S,3aS,7aR)-7-(bromomethylene)-octahydro-3a-methyl-1H-indene-3-yl}ethanone

https://huagongshe.com/reaction/1922632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
Reactant(S)-1-{(E,3S,3aS,7aR)-7-(bromomethylene)-octahydro-3a-methyl-1H-indene-3-yl}ethanolHCID 59456539—
CatalystHCID 178419074HCID 178419074—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-{(E,3S,3aS,7aR)-7-(bromomethylene)-octahydro-3a-methyl-1H-indene-3-yl}ethanoneHCID 59456514100.9%

Reaction Steps

Under a nitrogen atmosphere, a solution of (S)-1-{(E,3S,3aS,7aR)-7-(bromomethylene)-octahydro-3a-methyl-1H-indene-3-yl}ethanol (Compound 18: 58.1 mg, 0.2127 mmol) and N-methylmorpholine-N-oxide (37.4 mg, 0.3190 mmol) in acetonitrile (2 ml) was cooled in an ice bath, and tetra-n-propylammonium perruthenate (3.7 mg, 0.01064 mmol) was added thereto. The reaction mixture was stirred at the same temperature for 5 minutes, and at room temperature (22° C.) for 50 minutes, and the resulting mixture was diluted with ethyl acetate. The mixture was filtered through Celite, and the solids were washed with ethyl acetate, followed by evaporation of the filtrate under reduced pressure. The obtained crude product was purified by flash column chromatography to obtain 1-{(E,3S,3aS,7aR)-7-(bromomethylene)-octahydro-3a-methyl-1H-indene-3-yl}ethanone (58.2 mg, 100%). The spectrum data thereof agreed with the data described in Example 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173824B2
Source datasetuspto-grants-2012_05
ORD IDord-9acd7aebe6ee4f63901222cf8c23626e
Source noteuspto-grants-2012_05