HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hantzsch ester → 3-Hydroxy-2-(3-(2-((triisopropylsilyl)oxy)ethyl)benzyl)cyclopent-2-enone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hantzsch ester | HCID 70849 | — |
| Reactant | 1,3-Cyclopentanedione | HCID 77466 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | 3-(2-((Triisopropylsilyl)oxy)ethyl)benzaldehyde | HCID 54757655 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Hydroxy-2-(3-(2-((triisopropylsilyl)oxy)ethyl)benzyl)cyclopent-2-enone | HCID 54757863 | 76% |
Reaction Steps
To a solution of 14 (0.920 g, 3.0 mmol), 1,3-cyclopentadione (0.098 g, 1.0 mmol), and L-proline (0.005 mg) in dichloromethane (5 mL), diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate (0.253 g, 1.0 mmol) was added, and the resulting mixture was allowed to stir at rt for 12 h. The reaction mixture was directly purified by silica gel column chromatography using a gradient of ethyl acetate in hexanes as eluent, obtaining the title compound. Yield: 76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530520B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-aeec9718dc6944e796d68c0a7954f05e |
| Source note | uspto-grants-2013_09 |