Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 2,4,4-Trimethyl-1-pentene | HCID 7868 | — |
| Reactant | 1,2-Diethenylbenzene | HCID 66666 | — |
| Reactant | Phenol--2,4,4-trimethylpent-1-ene (1/1) | HCID 6455713 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-n-Octylphenol | HCID 15730 | — |
Reaction Steps
The reaction is performed discontinuously in a stirred flask equipped with contact thermometer and reflux condenser, under the conditions indicated in Table 1. The flask is charged with 90 g of a sulfonated polystyrene ion exchange resin in the H-form, crosslinked with divinylbenzene to an extent of 8% by weight and having an activity of 4.6 meg/g catalyst, and 282 g of phenol and 168 g of diisobutene (molar ratio phenol: diisobutene=2:1) and 9 g of water (2% by weight, based on the mixture of phenol-diisobutene) is added thereto. After a reaction period of 15 minutes, the crude product is separated from the catalyst by filtration and worked up by distillation in a manner known per se without any pretreatment, thus obtaining a p-octyl phenol having a very high degree of purity (setting point 80.2° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04461916 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-71d7e172a6ef44a2bf105fd824356454 |
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| Source note | uspto-grants-1984_07 |
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