HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384834Generated: October 30, 2026
Hydrochloric Acid → HCID 67119408, compound
https://huagongshe.com/reaction/384834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | HCID 86653605 | HCID 86653605 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Ethyl ketone | HCID 7288 | — |
| Product | HCID 67119408 | HCID 67119408 | 87.3% |
Reaction Steps
2-amino-4-methyl-5-(4-(trifluoromethoxy)phenoxy)benzoate (3.69 g), 20 ml of xylene, 5.3 ml of 3-pentanone, and 0.256 g of zinc chloride were added into a 50-ml glass flask equipped with a stirring device, a thermometer, a reflux condenser, and a Dean-Stark device under a nitrogen atmosphere, and the temperature was raised to reflux with stirring. A reaction was allowed to proceed for 50 hr while adding 1.1 g of zinc chloride in four divided portions. After the completion of the reaction, the mixture was cooled to 70° C., and 10 ml of 0.1 N hydrochloric acid was added to the cooled solution, followed by cooling to room temperature. The precipitated solid was collected on a suction filter, was washed with an aqueous methanol solution and distilled water, and was dried to give 2-ethyl-3,7-dimethyl-6-(4-(trifluoromethoxy)phenoxy)quinolin-4(1H)-one as a light brown solid (3.29 g, yield: 87.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367833B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-36ea1fca4f064646af12a4d2d1208a5d |
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| Source note | uspto-grants-2013_02 |
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