HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391360Generated: October 26, 2026
Ammonia → 2-hydroxy-4-(trifluoromethyl)benzamide
https://huagongshe.com/reaction/391360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Hydroxy-4-(trifluoromethyl)benzoic acid | HCID 164578 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-hydroxy-4-(trifluoromethyl)benzamide | HCID 286853 | — |
Reaction Steps
Thionyl chloride (2.7 mL) and N,N-dimethylformamide (0.1 mL) were added to a toluene (50.0 mL) solution of 4-trifluoromethylsalicylic acid (5.0 g), and the reaction mixture was refluxed for 30 minutes. The reaction mixture was left to cool. The reaction mixture was then added dropwise to aqueous ammonia (50.0 mL) under ice cooling, and the reaction mixture was stirred at the same temperature for 10 minutes. The pH of the reaction mixture was adjusted to 3 with concentrated hydrochloric acid, and the reaction mixture was then extracted with ethyl acetate. The organic layer was sequentially washed with water and a saturated brine and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluate; n-hexane:ethyl acetate=100:0 to 50:50). The title compound (1.84 g) was obtained as pale beige crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383839B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d5220478f95b4a688fdd5568ecff1681 |
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| Source note | uspto-grants-2013_02 |
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