HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580517Generated: November 2, 2026
3-(Trifluoromethyl)benzoic acid → HCID 14232986, compound
https://huagongshe.com/reaction/580517
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)benzoic acid | HCID 9963 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,4-Diaminoquinoline | HCID 1514289 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 14232986 | HCID 14232986 | 98.6% |
Reaction Steps
To a solution of 500 mg of 3-trifluoromethylbenzoic acid in 6 ml of anhydrous hexamethylphosphoramide (HMPA) and 0.6 ml of anhydrous acetonitrile is added dropwise 305 mg of thionyl chloride at -5°-0° C. under nitrogen. After stirring at the same temperature for 30 minutes, 380 mg of 3,4-diaminoquinoline is added and stirred at 0°-5° C. for 3 hours. The mixture is diluted with ice-water and neutralized with saturated aqueous sodium bicarbonate. The resulting crystals are filtered, washed with water, and dried to give 780 mg of 4-amino-3-(3-trifluoromethylbenzoylamino)quinoline B1 as a crude product. It is suspended in 15 g of polyphosphoric acid and heated at 120° C. for 4 hours with stirring. The mixture is poured into ice-water and neutralized with 1N sodium hydroxide. The resulting solid is filtered, washed with water and dried. It is chromatographed on silica gel with chloroform-methanol (10:1 v/v) as eluent, yielding 350 mg (47%) of C1 as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04753951 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-8b117dd8b5d44f5fb8586032ee787adf |
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| Source note | uspto-grants-1988_06 |
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