HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → Ethyl 8-(2-ethoxycarbonyl-5,6-dimethoxy-4,7-dioxoindan-2-yl)octanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ceric ammonium nitrate | HCID 180504 | — |
| Reactant | Ethyl 8-(2-ethoxycarbonyl-4,5,6,7-tetramethoxyindan-2-yl)octanoate | HCID 18348627 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 8-(2-ethoxycarbonyl-5,6-dimethoxy-4,7-dioxoindan-2-yl)octanoate | HCID 18348669 | 73.6% |
Reaction Steps
A water (1 ml) solution of CAN (342 mg, 0.624 mmols) was dropwise added to an acetonitrile (2 ml) solution of ethyl 8-(2-ethoxycarbonyl-4,5,6,7-tetramethoxyindan-2-yl)octanoate (100 mg, 0.208 mmols), with cooling with ice. The reaction mixture was stirred for 15 minutes and water was added thereto, which was then extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and then dried. The solvent was evaporated in vacuo, and the resulting crude product was purified by silica gel column chromatography (hexane only to hexane:ethyl acetate=4:1) to obtain the entitled compound (69 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06326369B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-16cbbbfdff9a429d9d88a05952b00d0d |
| Source note | uspto-grants-2001_12 |