HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703580Generated: October 30, 2026
Benzoyl chloride → (4-Butylphenyl)(phenyl)methanone
https://huagongshe.com/reaction/1703580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Butylbenzene | HCID 7705 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | (4-Butylphenyl)(phenyl)methanone | HCID 14148735 | 96.8% |
Reaction Steps
A 2.8 g (0.02 mole) of benzoic acid chloride was dissolved in 30 ml of carbon disulfide and then, 4.0 g (0.03 mole) of anhydrous aluminum chloride was added to the solution. A 2.68 g (0.02 mole) of n-butyl benzene was further added to the mixture with stirring, and the reaction was carried out at room temperature for 18 hours. Carbon disulfide was distilled off from the reaction mixture and water was added and the reaction product was extracted with benzene. The benzene phase was separated and washed with 1N-NaOH and with water and was dried with anhydrous sodium sulfate. The solvent was distilled off to obtain a pale yellow oily product. The oily product was distilled under a reduced pressure to obtain 4.6 g of 4-n-butyl benzophenone having a boiling point of 184° to 188° C./6 mmHg. (yield of 96.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04124726 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-ae7dc010e42c41988dc9d88c23ae4f11 |
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| Source note | uspto-grants-1978_11 |
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