HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248657Generated: October 29, 2026
1,4-Dichlorobenzene → 2,5-Dichlorobenzophenone
https://huagongshe.com/reaction/248657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dichlorobenzene | HCID 4685 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 2,5-Dichlorobenzophenone | HCID 458188 | 64% |
Reaction Steps
A mixture of 5.4 g of 1,4-dichlorobenzene, 4.2 g of aluminum chloride and 0.5 ml of benzoyl chloride was stirred at 170° C. Additional benzoyl chloride, up to a total of 4 g, was slowly added to the mixture over 2.5 hours, and the resulting mixture was stirred for another hour at 170° C. The molar ratio of reactants was 1.1/1.3/ (AClCl3 :Dichlorobenzene:Benzoyl Chloride). After work-up of the crude mixture as in Examples 7 through 10, 2,5-dichlorobenzophenone was obtained in 64% yield, as determined by gas chromatography using 3-chlorobenzophenone as the internal standard.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05210313 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-dbe583c0689442d1be02a717f513dd98 |
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| Source note | uspto-grants-1993_05 |
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