HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073470Generated: November 2, 2026
Hydrochloric Acid → HCID 131716693, compound
https://huagongshe.com/reaction/1073470
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butanoyl chloride, 2-methyl- | HCID 93697 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 22157312 | HCID 22157312 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | HCID 131716693 | HCID 131716693 | 54.1% |
Reaction Steps
Then, 4.0 g of (+)-2-methyl butanoyl chloride and 7 ml of nitrobenzene were charged into a flask and cooled to 0° C., added with 10.74 g (80 mmol) of anhydrous aluminum chloride and further with a solution of 4.97 g (19.6 mmol) of (+)-biphenyl-2-methylbutanoate in 9 ml of nitrobenzene, which was stirred at room temperature for 70 hours. After the addition of 2 normal hydrochloric acid and ice, the extraction with chloroform was performed. The extracted chloroform phase was washed with water, dried on anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified through a column chromatography of silica gel after distillation off of the solvent to obtain 3.60 g (yield: 54%) of an oily (+)-4-(2-methylbutanoyl) biphenyl-2-methylbutanoate. The NMR analytical values of this product were as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04970023 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-637f9b35957248cc84ddb4d48433ba59 |
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| Source note | uspto-grants-1990_11 |
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