HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzyl 4-formylpiperidine-1-carboxylate | HCID 2776272 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate | HCID 23435732 | — |
Reaction Steps
Methyl vinyl ketone (1.64 ml), ethanol (5 ml) and water (5 ml) were added to benzyl 4-formylpiperidine-1-carboxylate (5 g). The mixture was then added to a boiling solution of potassium hydroxide (0.22 g) in ethanol (10 ml) and the resulting reaction mixture was refluxed for 1 h (TLC control). When the reaction was complete, the mixture was added to water (25 ml) and extracted with ethyl acetate (2×50 ml). The combined organic phases were dried (Na2SO4) and concentrated in vacuo. The crude product obtained in this way was purified by column chromatography (silica gel, 25% ethyl acetate/hexane). Yield: 2.8 g (46%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455475B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-42f0456a8a0c49c8b6c2451fc354fb71 |
| Source note | uspto-grants-2013_06 |