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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191857Generated: November 2, 2026

Trifluoroacetic acid → HCID 11950812, compound

https://huagongshe.com/reaction/2191857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68963147HCID 68963147—
ProductHCID 11950812HCID 11950812—

Reaction Steps

Trifluoroacetic acid 5.0 mL was added to the obtained tert-butyl 2-((2-(dimethylamino)phenyl)amino)-4-phenylbenzoate, and it was stirred at room temperature for 3 hours. The solvent was removed under reduced pressure, the obtained residue was refined by reversed-phase silica gel column chromatography [eluent; 50-85% acetonitrile/0.1% trifluoroacetic acid aqueous solution], subsequently ethyl acetate and water were added to it, and it was adjusted to pH6.5 with saturated sodium hydrogen carbonate aqueous solution. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after washing with saturated sodium chloride aqueous solution, the solvent was removed under reduced pressure. Hexane was added to the obtained residue, and solid matter was filtrated to give 2-((2-(dimethylamino)phenyl)amino)-4-phenylbenzoic acid 17 mg of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-e96ac394bf0a40618cd44f49aef00380
Source noteuspto-grants-2012_12