Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 1,1,2,2-Tetrachloroethane | HCID 6591 | — |
| Reactant | Terephthalic Acid | HCID 7489 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | HCID 13115422 | HCID 13115422 | 50% |
Reaction Steps
To a mixture formed by adding 0.4 moles of AlCl3 to 0.6 mole of sym-tetrachloroethane are sequentially added, with stirring, 0.46 mole of nitromethane, 0.2 mole of terephthalic acid (reagent grade) and gradually 0.2 mole of phenol. The initial temperature of the resulting mixture is 25° C. and the temperature is raised to about 30° C. after 2 hours, then to about 40° C. after 4 hours, and about 1 hour later or until all HCl evolution is complete, the resulting mixture is allowed to stand overnight at room temperature. The mixture is treated with dilute sulfuric acid and the sym-tetrachloroethane is distilled from the mixture. The recovered solid is redissolved in boiling 10% Na2CO3, filtered, reprecipitated with concentrated HCl, and finally washed with water. About a 50% yield of 4-(4-hydroxybenzoyl) benzoic acid of good purity is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04906784 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-5d3f76b5ae884fa98c53516ff08dfe3e |
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| Source note | uspto-grants-1990_03 |
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