Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Alpha-Methylstyrene | HCID 7407 | — |
| Reactant | 2-Ethylhexanol | HCID 7720 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Product | Cumene | HCID 7406 | — |
| Product | Alpha-Methylstyrene | HCID 7407 | — |
| Product | 2-Ethylhexanol | HCID 7720 | — |
Reaction Steps
In the next step, a stainless steel autoclave was charged with the total amount of the above wet cake, 0.35 g of 5% palladium-carbon, 5.9 g of α-methylstyrene and 100 ml of 2-ethylhexanol and the internal atmosphere was replaced with nitrogen gas. The mixture was reacted at 180° C. for 3 hours, then cooled to 150° C. and filtered to recover the insoluble catalyst. 2-Ethylhexanol, α-methylstyrene and cumene formed by the reaction were distilled off from the filtrate under reduced pressure to obtain 33.6 g of 4,4'-biphenol as white crystals. The product had a purity of 98.2% based on liquid chromatography and contained 1.2% of p-phenylphenol as impurities. The yield of 4,4'-biphenol converted to a purity basis was 89% based on 4,4-bis(4-hydroxyphenyl)cyclohexanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04873374 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-f9a1fc8dcf9e48cb98b1a7abcd04cea9 |
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| Source note | uspto-grants-1989_10 |
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