HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014751Generated: October 31, 2026
4,4'-Dihydroxybiphenyl → 4,4'-Bis(octyloxy)-1,1'-biphenyl
https://huagongshe.com/reaction/1014751
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4,4'-Dihydroxybiphenyl | HCID 7112 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,4'-Bis(octyloxy)-1,1'-biphenyl | HCID 43833428 | 170% |
Reaction Steps
56 g of 4,4′-dihydroxybiphenyl was dissolved in 500 g ethanol. To this solution was added 40 g of potassium hydroxide, and the mixture was reacted. Next, this solution was heated, and 128 g of 1-bromooctane was dropped at 70° C., and subsequently, the mixture was reacted at 70° C. for 7 hours. The reaction was performed under a nitrogen atmosphere. After the reaction, this solution was cooled, and the generated precipitate was filtrated to recover. Next, this precipitate was washed with 500 ml of methanol, then, washed with a mixed solvent of methanol 500 ml/ion exchanged water 300 ml, and further, washed with a mixed solvent of acetone 500 ml/ion exchanged water 300 ml. This precipitate was dried under reduced pressure, to obtain 105 g of 4,4′-dioctyloxybiphenyl represented by the following structural formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07982212B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-2c1bfbbb8c744e90bad8ab4c340f20b8 |
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| Source note | uspto-grants-2011_07 |
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