Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-(4-Fluorophenyl)acetic acid | HCID 9837 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 54287785 | HCID 54287785 | — |
Reaction Steps
A mixture of 4-fluorophenylacetic acid (9 g, 58.4 mmol), 4-pyridinecarboxaldehyde (5.6 ml, 58.6 mmol), pyridine (6 ml) and acetic anhydride (6 ml) was heated at 150° C. for 1 h followed by evaporation and co-distillation with water. The resulting material crystallized on addition of ethanol. The solids were filtered and washed with ethanol and ethyl acetate to provide the title compound. MS (m/z): 244.0 (M+H)+; C14H10FNO2requir. 243.2 1H-NMR (DMSO-d6): d 8.43, 6.98 (2d, each 2H, Pyrid.), 7.73 (s, 1H, CH═), 7.21 (d, 4H, PhF).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410729B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-361d0a76f5a94fce952c723dbb4e8e4c |
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| Source note | uspto-grants-2002_06 |
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