HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883625Generated: November 1, 2026
8-Hydroxyquinoline → 1-(8-Hydroxyquinolin-5-yl)ethan-1-one--hydrogen chloride (1/1)
https://huagongshe.com/reaction/883625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-(8-Hydroxyquinolin-5-yl)ethan-1-one--hydrogen chloride (1/1) | HCID 20026880 | — |
Reaction Steps
8-hydroxyquinoline (500 gms/3.44 moles) was dissolved in ethylene chloride (5 lits) at 25-30° C. in an inert atmosphere. To this solution was added acetyl chloride (260 ml/4.12 moles) drop wise in 2 hours. The reaction mass was stirred for 15-20 minutes. Then, aluminum chloride (1.15 Kg/8.62 moles) was added in lots in 2 hours. The reaction mass was stirred at 25-30° C. for 15-20 minutes and heated to 70° C. for 13-14 hours. After completion of reaction, the reaction mass was cooled to 25-30° C. and slowly quenched in a mixture of crushed ice (10 Kg) and conc. HCl (500 ml). The resulting slurry was stirred for 15-20 minutes. The crude 5-acetyl-8-hydroxyquinoline hydrochloride was isolated by filtration, washed with 2 liters of acetone and dried under vacuum for 1 hour. Yield: 680 gms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236959B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-3f9312febbfd47ddb93d8b9e3342d2c0 |
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| Source note | uspto-grants-2012_08 |
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