Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Acetylpyridine | HCID 14286 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,5-Dimethoxybenzaldehyde | HCID 81747 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69677199 | HCID 69677199 | — |
Reaction Steps
To a well stirred solution of NaOH (12 g, 0.3 mmole) in H2O (125 ml) and methanol (250 ml) at 0° C. was added 3,5-dimethoxy benzaldehyde (19 g, 0.11 mmole) followed by a solution of 2-acetylpyridine (14.4 g, 0.12 mmole) in MeOH. The reaction was stirred at 0° C. for 1 hour and at room temperature for 16 hours. The precipitate was filtered and recrystallized from MeOH (Yield: 18 mg, 57%). The preparation scheme is shown below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06774082B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-08dfa7ab16c243c1be13c7d91a2ab152 |
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| Source note | uspto-grants-2004_08 |
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