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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922630Generated: November 2, 2026

(S)-1-{(3S,3aS,7S,7aR)-octahydro-7-hydroxy-3a-methyl-1H-indene-3-yl}ethyl formate → (S)-1-{(3S,3aR,7aR)-octahydro-3a-methyl-7-oxo-1H-indene-3-yl}ethyl formate

https://huagongshe.com/reaction/1922630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-1-{(3S,3aS,7S,7aR)-octahydro-7-hydroxy-3a-methyl-1H-indene-3-yl}ethyl formateHCID 59456545—
CatalystHCID 178419074HCID 178419074—
SolventAcetonitrileHCID 6342—
Product(S)-1-{(3S,3aR,7aR)-octahydro-3a-methyl-7-oxo-1H-indene-3-yl}ethyl formateHCID 5945652797%

Reaction Steps

Under a nitrogen atmosphere, a solution of (S)-1-{(3S,3aS,7S,7aR)-octahydro-7-hydroxy-3a-methyl-1H-indene-3-yl}ethyl formate (Compound 16: 899.6 mg, 3.975 mmol) in acetonitrile (10 ml) was cooled in an ice bath, and tetra-n-propylammonium perruthenate (35 mg, 0.0994 mmol) was added thereto. The reaction mixture was stirred in the ice bath for 3 minutes, and at room temperature (23° C.) for 45 minutes. The reaction mixture was filtered through Celite, and the resulting mixture was washed with ethyl acetate, followed by evaporation under reduced pressure. The crude product was purified by flash column chromatography to obtain (S)-1-{(3S,3aR,7aR)-octahydro-3a-methyl-7-oxo-1H-indene-3-yl}ethyl formate (865.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173824B2
Source datasetuspto-grants-2012_05
ORD IDord-de8d62fd49dd4613a1405121d984b87b
Source noteuspto-grants-2012_05