HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421056Generated: November 1, 2026
Hydrochloric Acid → 2-Hydroxy-5-phenyl-n[3,5-bis(trifluoromethyl)phenyl]benzamide
https://huagongshe.com/reaction/421056
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-iodo-benzamide | HCID 11190699 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Hydroxy-5-phenyl-n[3,5-bis(trifluoromethyl)phenyl]benzamide | HCID 11750632 | 61.1% |
Reaction Steps
N-[3,5-Bis(trifluoromethyl)phenyl]-2-hydroxy-5-iodobenzamide (200 mg, 0.42 mmol) was dissolved in 1,2-dimethoxyethane (3 mL). Tetrakis(triphenylphosphine)palladium (16 mg, 0.0014 mmol) was added under argon atmosphere, and the mixture was stirred at room temperature for 5 minutes. Then dihydroxyphenylborane (57 mg, 0.47 mmol) and 1M sodium carbonate (1.3 mL) were added and refluxed for 2 hours. After cooling to room temperature, the reaction mixture was poured into diluted hydrochloric acid and extracted with ethyl acetate. After the ethyl acetate layer was washed with water and brine one after another, dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=6:1→3:1) to give the title compound (109 mg, 61.1%) as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097759B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-89b7e5e0ad79411884d12cf1e3229ec1 |
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| Source note | uspto-grants-2012_01 |
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