Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Chloro-6-fluorobenzaldehyde | HCID 67847 | — |
| Product | HCID 8854025 | HCID 8854025 | 28% |
Reaction Steps
A mixture of 2-chloro-6-fluorobenzaldehyde (0.599 g, 3.8 mmol) and 1-phenylethanone (0.414 mL, 0.38 mmol) in piperidine (1 mL) was heated at 100° C. for 1 h. The reaction mixture was allowed to cool to rt and was concentrated. The residue was purified by column chromatography to give (2E)-3-(2-chloro-6-fluorophenyl)-1-pyridin-3-ylprop-2-en-1-one (0.28 g, 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795249B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-c4267a4f7e834504ac75b767481e5d3d |
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| Source note | uspto-grants-2010_09 |
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