HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51974Generated: October 26, 2026
3-Nitroaniline → 4'-Trifluoromethyl-biphenyl-2-carboxylic acid (3-nitro-phenyl)-amide
https://huagongshe.com/reaction/51974
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Nitroaniline | HCID 7423 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chloride | HCID 11066000 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Trifluoromethyl-biphenyl-2-carboxylic acid (3-nitro-phenyl)-amide | HCID 10156957 | 100% |
Reaction Steps
To a solution of 3-nitroaniline (28.8 g, 209 mmol, 1 equiv) in THF (1000 mL, 35 volumes), was added triethylamine (70 mL, 500 mmol, 2.4 equiv). 3-Nitroaniline can be obtained from Aldrich, Milwaukee, Wis. A solution of 4′-trifluoromethyl-biphenyl-2-carbonyl chloride (71.3 g, 250 mmol, 1.2 equiv) in THF (250 mL, 3.5 volumes) was added dropwise over 30 minutes. The reaction was stirred at room temperature for 48 hours. The slurry was then filtered through diatomaceous earth and the filtrate was concentrated. Water (700 mL, 24 volumes) was added and the slurry was stirred at room temperature for 12 hours. The solids were collected by filtration and dried under vacuum at 40° C. to provide 4′-trifluoromethyl-biphenyl-2-carboxylic acid (3-nitro-phenyl)-amide (80.7 g, 100%) as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713489B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-2927607f630a4bbc812d4fbdab602dd2 |
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| Source note | uspto-grants-2004_03 |
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