HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372675Generated: October 26, 2026
1-Octanol → Octyl 4'-hydroxy-4-biphenylcarboxylate
https://huagongshe.com/reaction/2372675
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4'-Hydroxy-4-biphenylcarboxylic acid | HCID 301556 | — |
| Solvent | Water | HCID 962 | — |
| Product | Octyl 4'-hydroxy-4-biphenylcarboxylate | HCID 14692993 | 87.5% |
Reaction Steps
Fifteen grams of n-octanol, 7.5 g of 4-(4'-hydroxyphenyl)benzoic acid and 7.0 g of p-toluene-sulfonic acid were dissolved with 100 ml of toluene in a three necked flask with a dehydration, apparatus, and the mixture was refluxed for 15 hours. Water was added to the mixture to separate a toluene layer. Ten grams of 4-(4'-octyloxycarbonylphenyl)phenol (AB) were obtained by removing the toluene layer under reduced pressure followed concentration. (s)-4-(1-chloro-2-methylpropylcarbonyloxy)benzoic acid dispersed in 20 ml of carbon tetrachloride was reacted with 5 ml of thionyl chloride by refluxing for 3 hours. After removing the solvent (s)-4-(1-chloro-2-methylpropylcarbonyloxy)benzoic chloride (AC) was obtained. 1.5 g of (AC) was dissolved with mixed solvent of 80 ml of carbon tetrachloride and 10 ml of pyridine, and then 1.7 g of (AB) was added to the mixed solution with cooling and the mixture was allowed to stand overnight to obtain crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05100579 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-3738d345859b4867a0d30536a1963626 |
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| Source note | uspto-grants-1992_03 |
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