Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Phenol, o-(alpha,alpha-dimethylbenzyl)- | HCID 123377 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22290015 | HCID 22290015 | — |
Reaction Steps
Cumylphenyl benzoate is prepared in accordance with the following procedure: one mole of cumylphenol was dissolved in 600 ml of benzene containing 1.2 moles of triethylamine in a 2-liter stirred glass reactor equipped with external heating and cooling devices. The reaction mass was cooled to and maintained at 15°-20° C. during the addition of 1.1 moles of benzoyl chloride over a period of 1.5 hours. After completion of addition, the resulting slurry was heated to and maintained at 40°-45° C. for 1 hour, and thereafter cooled to ambient temperature and filtered. The filter cake was washed with 200 ml of toluene and the combined washings and filtrate distilled to give 214.9 g (68 mole %) of a pale yellow oil having a boiling point at 0.5 mm Hg of 261°-265° C., a specific gravity at 55° C. of 1.082, and a viscosity at 55° C. of 215 cps. On standing, the oil solidified to form a white solid having a melting point of 43°-46.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04199517 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-24bcd67e088847c3b783e69e98c16ff1 |
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| Source note | uspto-grants-1980_04 |
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