HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286703Generated: November 3, 2026
Acetic Acid → 2-(trifluoromethyl)quinoline-4-carboxylic acid
https://huagongshe.com/reaction/2286703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isatin | HCID 7054 | — |
| Reactant | Methyl trifluoromethyl ketone | HCID 9871 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(trifluoromethyl)quinoline-4-carboxylic acid | HCID 9547712 | 76% |
Reaction Steps
A 500 mL three-necked flask equipped with a stirrer, water condenser and thermometer was charged with fifteen grams (15 g) of isatin (0.10 mol), six grams (6 g) of potassium hydroxide (0.11 mol), and 100 mL of water. About 12 grams (12 g) of glacial acetic acid (0.20 mol) and 12 grams (12 g) of sodium acetate (0.14 mol) were then added to bring the pH of the mixture to 5±0.1. After the addition of 13.7 grams of trifluoroacetone (0.12 mol), the mixture was heated to 70° C. for 15 hours. At the end of this time, the mixture was acidified with 10% hydrochloric acid. A precipitate of 2-trifluoromethyl cinchoninic acid was obtained which was separated by filtration. The precipitate was washed with water until the wash water was clear, and then dried in air. About 18.8 grams of product was recovered, representing a yield of 76 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04267333 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-a33f0ae5408a46798cca823cdce92bc4 |
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| Source note | uspto-grants-1981_05 |
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