HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846559Generated: October 31, 2026
Hydrochloric Acid → (+)-2-Methyloctanoic acid 4-(2-methyloctanoyl) biphenyl
https://huagongshe.com/reaction/846559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-Methyl octanoic acid chloride | HCID 12812232 | — |
| Reactant | (+)-2-Methyloctanoic acid biphenyl | HCID 67826054 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | (+)-2-Methyloctanoic acid 4-(2-methyloctanoyl) biphenyl | HCID 67913760 | 49% |
Reaction Steps
Next, 2.02 g (11.4 mmol) of the above (+)-2-methyloctanoic acid chloride and 3 ml of nitrobenzene were charged into a flask, and cooled to 0° C., to which was added 3.06 g (22.9 mmol) of anhydrous aluminum chloride with stirring and then the resulting mixture was stirred at room temperature for 30 minutes. This mixture was added with a solution of 2.89 g (7 mmol) of (+)-2-methyloctanoic acid biphenyl dissolved in 3 ml of nitrobenzene, which was reacted at room temperature for 140 hours with stirring. After the completion of the reaction, 2N hydrochloric acid and ice were added, and the extraction with chloroform was carried out, and the extract was washed with water, dried on anhydrous magnesium sulfate, distilled to remove the solvent, and purified by a column chromatography of silica gel to obtain 1.55 g (yield 49%) of an oily (+)-2-methyloctanoic acid-4-(2-methyloctanoyl) biphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137653 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-e4d8a46715dd4bb5804583d7414ffe70 |
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| Source note | uspto-grants-1992_08 |
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