HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36824Generated: October 25, 2026
Acetyl chloride → 1-Acetyl-4-(4-phenylphenyl)benzene
https://huagongshe.com/reaction/36824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | O-Terphenyl | HCID 6766 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-Acetyl-4-(4-phenylphenyl)benzene | HCID 3744472 | 119% |
Reaction Steps
After a mixture of 172 g of terphenyl, 860 ml of benzene, and 353 g of acetyl chloride was cooled to -5° C., it was added with a total of 200 g of anhydrous aluminium chloride in few instalments, and subjected to reaction at -5° C. for 1 hour and further at 10° C. for 1 hour. The solid materials thus formed were separated by filtration, washed with a total of 4 liter of methanol in few instalments, and then recrystallized from chloroform to obtain 121 g of 4-acetyl-p-terphenyl, 2. The yield was 59%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05417885 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-fcf69c324b7543df958050b25c92f785 |
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| Source note | uspto-grants-1995_05 |
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