HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51975Generated: October 30, 2026
Tetrahydrofuran → 4'-Trifluoromethyl-biphenyl-2-carboxylic acid (3-amino-phenyl)-amide
https://huagongshe.com/reaction/51975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4'-Trifluoromethyl-biphenyl-2-carboxylic acid (3-nitro-phenyl)-amide | HCID 10156957 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4'-Trifluoromethyl-biphenyl-2-carboxylic acid (3-amino-phenyl)-amide | HCID 9924828 | 94% |
Reaction Steps
Ammonium formate (16.3 g, 258 mmol, 3 equiv), followed by Pearlman's catalyst [Pd(OH)2] (6.03 g, 4.30 mmol, 0.05 equiv) was added to a solution of 4′-trifluoromethyl-biphenyl-2-carboxylic acid (3-nitro-phenyl)-amide (33.2 g, 85.9 mmol, 1 equiv) in isopropanol (330 mL, 10 volumes) and ethyl acetate (170 mL, 5 volumes). The mixture was heated at reflux for 3 hours. After cooling, THF (500 mL) was added to the reaction mixture to help solublize the product. The reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated to about 100 mL. ethyl acetate (600 mL) and THF (200 mL) were added. The organic layer was washed with saturated sodium bicarbonate solution (300 mL), dried over sodium sulfate, filtered, and concentrated to afford 4′-trifluoromethyl-biphenyl-2-carboxylic acid (3-amino-phenyl)-amide (28.7 g, 94%) as an off-white solid.
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-6082b665eb834a19a1f9cd71e7d72b24 |
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| Source note | uspto-grants-2004_03 |
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