HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485399Generated: October 31, 2026
Methane → 2-Bromo-4'(-p-tolyl)acetophenone
https://huagongshe.com/reaction/485399
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | 4-Methylbiphenyl | HCID 12566 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 2-Bromo-4'(-p-tolyl)acetophenone | HCID 13531978 | — |
Reaction Steps
An 11.7 g. portion of 4-methylbiphenyl was dissolved in 75 ml. of carbon disulfide and cooled in an ice bath while 11.6 g. of aluminum chloride was added portionwise with vigorous stirring. A 15.9 g. portion of bromoacetylbromide was added dropwise and after completion and the reaction subsided the mixture was heated at reflux for 3 hours, then cooled overnight. The mixture was poured into crushed ice and 150 ml. of acetic acid and stirred for 1.5 hours. The resulting gum was collected and stirred in methanol for 2 hours, giving a solid. This solid was dissolved in methanol:acetone, treated with charcoal and cooled. The solution was decanted, concentrated to about 150 ml., decanted and recooled giving a solid which was collected, giving the desired intermediate as a beige solid, m.p. 120°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536517 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-99dfa56c9f034ce6bfea04b037919035 |
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| Source note | uspto-grants-1985_08 |
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