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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantIsatinHCID 7054—
ReactantMethyl trifluoromethyl ketoneHCID 9871—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium AcetateHCID 517045—
SolventWaterHCID 962—
Product2-(trifluoromethyl)quinoline-4-carboxylic acidHCID 954771276%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267333
Source datasetuspto-grants-1981_05
ORD IDord-a33f0ae5408a46798cca823cdce92bc4
Source noteuspto-grants-1981_05