HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845316Generated: October 31, 2026
p-Toluenesulfonic acid → HCID 14303913, compound
https://huagongshe.com/reaction/845316
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,5-Dimethoxyaniline | HCID 66301 | — |
| Reactant | HCID 19847704 | HCID 19847704 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 14303913 | HCID 14303913 | — |
Reaction Steps
To 200 ml of chlorobenzene were added 3.1 g (0.01 mole) of 1-(4-methoxyphenyl)-2-methyl-5-phenyl-1,3,5-pentanetrione, 2.3 g (1.5 mole) of 3,5-dimethoxyaniline, 2.9 g (0.015 mole) of para-toluenesulfonic acid and 10 g of Molecular Sieves 5A, followed by refluxing the resulting mixture for 2 hours. After cooling the reaction mixture, solid matter was removed from the reaction mixture, followed by addition of 500 ml of chloroform thereto. The organic layer was washed first with 200 ml of 10% hydrochloric acid and then with water. The organic layer was then dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate by filtration, the solvent was distilled off and the residue was subjected to chromatography on a silica gel column (eluent: ethyl acetate). Upon washing the resultant crystals with ethyl acetate, 3.3 g of 1-(3,5-dimethoxyphenyl)-2-(4-methoxyphenyl)-3-methyl-6-phenyl-4(1H)-pyridinone p-toluenesulfonate having a melting point of 202°-204° C. was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04757081 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-5a0cc821c9bf4e0583c75addd122033b |
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| Source note | uspto-grants-1988_07 |
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