HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679796Generated: October 30, 2026
3-Nitroaniline → 2-(3-trifluoromethylphenoxy)N-(3-nitrophenyl)nicotinamide
https://huagongshe.com/reaction/1679796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Nitroaniline | HCID 7423 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(3-Trifluoromethylphenoxy)nicotinoyl chloride | HCID 11162424 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(3-trifluoromethylphenoxy)N-(3-nitrophenyl)nicotinamide | HCID 12894406 | — |
Reaction Steps
A solution of 1.5 grams (0.011 mole) 3-nitroaniline and 1.0 gram (0.011 mole) triethylamine in 100 milliliters toluene was placed in a flask. There was slowly added, with stirring, a solution of 3.2 grams (0.011 mole) 2-(3-trifluoromethylphenoxy) nicotinoyl chloride in 25 milliliters toluene. The rate of addition was controlled so as to maintain the temperature below 35° C. After the addition was complete the mixture was stirred at 45° C. for one hour, cooled, poured into 100 milliliters toluene, and washed with two 150-milliliter portions of water. The organic phase was separated, dried with magnesium sulfate, filtered and the solvent removed to produce 3.3 grams (73.3% of theoretical yield) of the desired product, m.p. 90°-95° C. The structure was confirmed by mass spectrometry.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04270946 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-63b7610a4b5049fa84b211cb46f590eb |
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| Source note | uspto-grants-1981_06 |
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