Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2-Propynoic acid, 3-phenyl-, ethyl ester | HCID 91516 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-(4-fluorophenyl)-1-phenylpropaneimine | HCID 14726141 | — |
| Product | HCID 14303555 | HCID 14303555 | — |
Reaction Steps
To 300 ml of toluene were added 9.1 g (0.040 mole) of N-(4fluorophenyl)-1-phenylpropaneimine, 4.7 g (0.035 mole) of aluminum chloride and 5.2 g (0.030 mole) of ethyl phenylpropiolate, followed by refluxing the resultant mixture for 5 hours. Thereafter, the reaction mixture was poured into 500 ml of 2N sulfuric acid which had been ice-cooled, followed by extraction with chloroform. After washing the organic layer with water, the organic layer wad dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate, the solvent was distilled off and the residue was purified by chromatography on a silica gel column (eluent: 1:50 mixed solvent of methanol and chloroform). The resultant crystals were recrystallized from 1:1 mixed solvent of acetone and hexane to give 1.0 g of 1-(4-fluorophenyl)-3-methyl-2,6-diphenyl-4(1H)-pyridinone having a melting point of 256°-259° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04871751 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-dfd91291af1243c0a38ec9e6f2463d95 |
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| Source note | uspto-grants-1989_10 |
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