HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646600Generated: October 30, 2026
4'-Methoxyacetophenone → HCID 59215170, compound
https://huagongshe.com/reaction/646600
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4'-Methoxyacetophenone | HCID 7476 | — |
| Reactant | 2,6-Dichloronicotinic acid | HCID 854047 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59215170 | HCID 59215170 | 63% |
Reaction Steps
Elemental sodium (173 mg, 7.5 mmol) was added to 40 mL of absolute EtOH stirring under nitrogen. After all of the sodium reacted, 4-methoxyacetophenone (1.44 g, 7.5 mmol) was added, and the reaction stirred an additional 15 minutes . 2,6-Dichloronicotinic acid (1 g, 5.2 mmol) and copper acetate (80 mg, 0.65 mmol) was added and the reaction was stirred at reflux for 16 hours. The reaction was cooled to room temperature and quenched with 1 mL concentrated acetic acid. The mixture was concentrated to a solid, and redissolved in EtOAc. A small portion of fine inorganic precipitate was filtered off. The organic layer was extracted with 3×100 mL 1N NaOH. This was acidified with 1 N HCl to a pH of ˜4. A precipitate formed and was collected by vacuum filtration, yielding 6-chloro-2-[2-(4-methoxyphenyl)-2-oxo-ethyl]-nicotinic acid (1 g, 63%) as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705151B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-158243610cd34a66a8ee61fb003def2c |
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| Source note | uspto-grants-2010_04 |
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