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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384360Generated: November 3, 2026

Hydrochloric Acid → 2-Hydroxy-5-phenyl-n[3,5-bis(trifluoromethyl)phenyl]benzamide

https://huagongshe.com/reaction/2384360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantN-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-iodo-benzamideHCID 11190699—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Hydroxy-5-phenyl-n[3,5-bis(trifluoromethyl)phenyl]benzamideHCID 1175063261.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263657B2
Source datasetuspto-grants-2012_09
ORD IDord-0a1bb76e48bb4c21ad58bb3258a9e7ec
Source noteuspto-grants-2012_09