HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284282Generated: October 31, 2026
Hydrochloric Acid → 1-(4-Bromophenyl)-2-hydroxy-2-p-tolylethanone
https://huagongshe.com/reaction/1284282
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(4-Bromophenyl)-2-oxoacetaldehyde | HCID 233586 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Bromophenyl)-2-hydroxy-2-p-tolylethanone | HCID 20372296 | — |
Reaction Steps
A solution of 67 g. (0.314 mole) of p-bromophenyl-glyoxal in 300 ml. of dry toluene is added dropwise over 1 1/2 hours to a stirred suspension of 84 g. (0.6 mole) of anhydrous aluminum chloride in 1.25 l. of dry toluene cooled in an ice-bath. Stirring in the cold is continued for 5 hours and the mixture then is held at 5°-10°C. overnight. The mixture is poured into about 2 l. of ice and 6N hydrochloric acid. The aqueous phase is separated and re-extracted with three portions of benzene. The combined, washed and dried organic extracts are concentrated under reduced pressure to a volume of about 200 ml. Dilution with 150 ml. of petroleum ether precipitates the white crystalline product, m.p. 80°-82°C. Repeated recrystallization from 60% ethanol affords the analytical sample, m.p. 82°-83.5°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03978127 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-9d4402a11cc64c9696b16e7ed40c9a92 |
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| Source note | uspto-grants-1976_08 |
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