Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 2-Propenoic acid, 3-(4-nitrophenyl)- | HCID 70156 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Phenyl p-nitrocinnamate | HCID 47098254 | — |
Reaction Steps
Phosphorus pentachloride (22 g) was added to 19.3 g of p-nitrocinnamic acid suspended in 300 ml of ethyl acetate, and the resulting mixture was stirred at room temperature for 1 hour. After the reaction, the solvent was distilled off under reduced pressure, upon which p-nitrocinnamoyl chloride precipitated. The precipitates thus obtained were dissolved in 300 ml of ethyl acetate, and 9.4 g of phenol was added to the resulting solution, after which 12 g of triethylamine was slowly added thereto at room temperature with stirring. After reaction at room temperature for 1 hour, the reaction mixture was washed with 10% HCl, 10% NaOH and water in this order and dried on anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure, to obtain phenyl p-nitrocinnamate. Yield: 25.5 g (95%); melting point: 151°-152° C.; IR (cm-1): 1720, 1529, 1345.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04182897 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-25433df8ae75466096480618c0805963 |
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| Source note | uspto-grants-1980_01 |
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