HuagongsheHuagongshe Chemistry Print Report · For research reference only
(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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-1-{(3S,3aS,7S,7aR)-octahydro-7-hydroxy-3a-methyl-1H-indene-3-yl}ethyl formate | HCID 59456545 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-1-{(3S,3aR,7aR)-octahydro-3a-methyl-7-oxo-1H-indene-3-yl}ethyl formate | HCID 59456527 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173824B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-de8d62fd49dd4613a1405121d984b87b |
| Source note | uspto-grants-2012_05 |