HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618910Generated: November 1, 2026
Hydrochloric Acid → 7,8-Difluoro-2-methylquinolin-3-ol
https://huagongshe.com/reaction/1618910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6,7-Difluoro-1H-indole-2,3-dione | HCID 22274399 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7,8-Difluoro-2-methylquinolin-3-ol | HCID 68287863 | — |
Reaction Steps
After 41 g of the crude product of 6,7-difluoroisatin was added to 200 mL of water, 75.3 g of potassium hydroxide (6 equivalents) was added thereto under ice-cooling and the mixture was stirred for 30 minutes. 42 g of bromoacetophenone (1.4 equivalents) was added dropwise to the suspension while maintaining the internal temperature of the reaction solution at 20 to 25° C., and the mixture was further stirred overnight at room temperature. After the resultant was neutralized with concentrated hydrochloric acid, the precipitated crystals were collected by filtration and washed with a small amount of water. The thus obtained crystals were sufficiently dried, and then added little by little to 100 mL of nitrobenzene heated to 130 to 140° C., and the mixture was stirred further for 1 hour at 150° C. After the reaction solution was cooled to room temperature, the precipitated crystals were washed with chloroform to obtain 26.3 g of 7,8-difluoro-3-hydroxy-2-methylquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772200B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-edddf675a1804c4e8137d59eef8574a4 |
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| Source note | uspto-grants-2014_07 |
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