Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 13416605 | HCID 13416605 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-pyridyl)cyclopentene | HCID 12217802 | 52.5% |
Reaction Steps
In an autoclave, 60.0 g (368 mM) of 1-hydroxy-2-(2-pyridyl)cyclopentane was placed and stirred for 60 hours at 170° C., followed by cooling, addition of water and extraction with methylene chloride. The organic layer was dried with anhydrous sodium sulfate, followed by distilling-off of the solvent under reduced pressure and then purification by silica gel column chromatography (eluent: hexane/ethyl acetate=8/1) to obtain 28.0 g of liquid 1-(2-pyridyl)cyclopentene (Yield: 52.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06733905B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-88c005ed4bf74721916cefb4506249f3 |
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| Source note | uspto-grants-2004_05 |
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