HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846555Generated: October 25, 2026
Hydrochloric Acid → 2-Methylbutanoic acid 4-(2-methylbutanoyl) biphenyl
https://huagongshe.com/reaction/846555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Butanoyl chloride, 2-methyl- | HCID 93697 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 2-Methylbutanoic acid 4-(2-methylbutanoyl) biphenyl | HCID 67913765 | 54% |
Reaction Steps
Then, 4.0 g of (+)-2-methylbutanoic acid chloride and 7 ml of nitrobenzene were charged into a flask and cooled to 0° C., to which was added 10.74 g (80 mmol) of aluminum chloride with stirring and further added a solution of 4.97 g (19.6 mmol) of (+) 2-methylbutanoic acid-4-biphenyl in 9 ml of nitrobenzene and then stirred at room temperature for 70 hours. Thereafter, the resulting mixture was added with 2 normal hydrochloric acid and ice and extracted with chloroform. The chloroform layer was washed with water, dried on anhydrous magnesium sulfate, and purified by a column chromatography of silica gel after the distillation off of the solvent to obtain 3.60 g (yield 54%) of oily 2-methylbutanoic acid-4-(2-methylbutanoyl) biphenyl. The NMR analytical values of this purified product were as follows.
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-58e799445db4465e80ac4d17f7d08dc9 |
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| Source note | uspto-grants-1992_08 |
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