HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-(Methylcarbonyloxy-methyl)-5-(1-acenaphthyl)-spiro[indoline-3,4'-piperidin]-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-acenaphthene | HCID 13634446 | — |
| Reactant | 1-(Methoxycarbonylmethyl)-spiro[indoline-3,4'-piperidin]-2-one | HCID 59164537 | — |
| Product | 1-(Methylcarbonyloxy-methyl)-5-(1-acenaphthyl)-spiro[indoline-3,4'-piperidin]-2-one | HCID 68545128 | — |
Reaction Steps
1-Bromo-acenaphthene (0.022 g, 0.093 mmol) and 1-(methoxycarbonylmethyl)-spiro[indoline-3,4′-piperidin]-2-one (0.013 g, 0.046 mmol) were dissolved in dry N,N-dimethylformamide (1 mL). Potassium carbonate (0.02 g, 0.14 mmol) was then added and the reaction mixture was stirred at room temperature under a nitrogen atmosphere for 18 hours. The reaction mixture was partitioned with water and ethyl acetate. The organic layer was washed with brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield a crude oil. The crude oil was purified via flash chromatography (5% methanol/dichloromethane) to yield the title compound as a foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07655670B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-b4863591d39542a7abd8812fb145e4ff |
| Source note | uspto-grants-2010_02 |