HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255637Generated: October 31, 2026
Chloranil → Methyl 1-(4-hydroxyphenyl)-6-(2-naphthyl)-4-oxo-1,4-dihydronicotinate
https://huagongshe.com/reaction/255637
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloranil | HCID 8371 | — |
| Reactant | HCID 178500767 | HCID 178500767 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 1-(4-hydroxyphenyl)-6-(2-naphthyl)-4-oxo-1,4-dihydronicotinate | HCID 15590992 | 44.4% |
Reaction Steps
In 12 ml of N,N-dimethylformamide was dissolved 1.7 g of methyl 2-(4-hydroxyphenylaminomethylene)-5-(2-naphthyl)-3-oxo-4-pentenoate, and they were reacted at 140° C. for 2 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and the residue was purified by a column chromatography (Wako Silica Gel C-200; eluent: chloroform/methanol (19:1 by volume) mixture). The purified oily substance was dissolved in 15 ml of dioxane and the resulting solution was heated to 80° C. To this solution was added dropwise at 80° C. a solution formed by dissolving 1.1 g of 2,3,5,6-tetrachloro-p-benzoquinone in 15 ml of dioxane. After this addition was completed, the solvent was removed by distillation under reduced pressure, and to the residue was added 20 ml of a chloroform/methanol (5:1 by volume) mixed solvent. The crystals thus formed were collected by filtration, washed with 5 ml of the same mixed solvent as mentioned above, and then dried to obtain 0.75 g of methyl 1-(4-hydroxyphenyl)-6-(2-naphthyl)-4-oxo-1,4-dihydronicotinate having a melting point of 280° C. or more.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04698352 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-53b066261acc4f0aa776a263e0bb2673 |
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| Source note | uspto-grants-1987_10 |
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