Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Ethylhexanoic Acid | HCID 8697 | — |
| Reactant | HCID 12759835 | HCID 12759835 | — |
| Product | HCID 20340180 | HCID 20340180 | — |
Reaction Steps
Cumylphenyl 2-ethylhexanoate was prepared in accordance with the following procedure: a 2-liter flask equipped with a mechanical agitator, a ten theoretical plate fractionating column, an automatic reflux splitter pot, vapor thermo-controllers, a condenser, receivers, and external heating and cooling devices, was charged with 2 moles of cumylphenyl acetate, 5 moles of 2-ethylhexanoic acid and 5 grams of 98% sulfuric acid. Heat was supplied externally and the distillate was collected at a 20:1 reflux ratio at a vapor temperature below 120° C. at atmospheric pressure. A total of 64 cc of distillate was collected in 24 hours. The residual pot contents were cooled to ambient temperature and extracted 5 times with 2 l. of 8% sodium bicarbonate dried over anhydrous Na2SO4 and fractionated to give 408 g. (58 mole %) of a pale yellowish oil. The oil had a boiling point at 0.2 mm Hg of 252°-257° C., a specific gravity 20/20 of 1.045 and a saponification value of 2.82 meq/g. The cumylphenyl 2-ethylhexanoate ester has a theoretical saponification value of 2.85 meq/g.
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-6b5269eac7144991ba9430a48341ef94 |
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| Source note | uspto-grants-1980_04 |
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