HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369919Generated: October 29, 2026
3a-Fluoro-7-(2-furanyl)-1,2,3,3a,5,9b-hexahydrocyclopenta[c]quinolin-4-one → HCID 18516392, compound
https://huagongshe.com/reaction/1369919
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3a-Fluoro-7-(2-furanyl)-1,2,3,3a,5,9b-hexahydrocyclopenta[c]quinolin-4-one | HCID 18516356 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Catalyst | Ruthenium dioxide | HCID 82848 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | water acetonitrile CCl4 | HCID 22592919 | — |
| Product | HCID 18516392 | HCID 18516392 | — |
Reaction Steps
A suspension of 0.5 g (1.8 mmol) of 3a-fluoro-7-(2-furanyl)-1,2,3,3a,5,9b-hexahydrocyclopenta[c]quinolin-4-one in 63 ml of acetonitrile-carbon tetrachloride-water (2:1:2) is mixed with 5.9 g (27.6 mmol) of sodium periodate and 0.05 g (0.4 mmol) of ruthenium(IV) oxide, and it is stirred for 4 hours at room temperature. The batch is diluted with water and extracted with ethyl acetate. The combined extracts are dried (Na2SO4) and concentrated by evaporation in a vacuum. The residue is taken up in 0.5 M potassium hydroxide solution. This solution is washed with methyl-tert-butyl ether, acidified with concentrated hydrochloric acid and extracted with ethyl acetate. The combined extracts are dried (Na2SO4) and concentrated by evaporation in a vacuum: 0.31 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06579883B1 |
|---|
| Source dataset | uspto-grants-2003_06 |
|---|
| ORD ID | ord-54846ee6f61646b99bf1e691172f9d96 |
|---|
| Source note | uspto-grants-2003_06 |
|---|